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1.
Summary The lymphocytes of the rat thymus can be grossly differentiated by their cell membrane-bound proteinases. Subcapsular thymocytes lack aminopeptidase A (APA) and AMP and -glutamyltranspeptidase (GGT). Cortical thymocytes show a high activity of APA but no APM and no GGT. Medullar thymocytes posses a high GGT and APM activity but are free of APA. Under Mg deficiency, the APA-negative subcapsular thymocytes are reduced. In lymphoma and beginning lymphoma, APA, APM and GGT are absent. In lymphoma, the alkaline phosphatase activity is increased. Differences are found for dipeptidylpeptidase IV (DPP IV). In some lymphoma, its activity is reduced, in others the DPP IV activity is increased.  相似文献   

2.
Summary The distribution of activities of membrane aminopeptides (aminopeptidases M (APM), aminopeptidase A (APA), dipeptidyl peptidase IV (DPP IV), -gluamyltransferase (GGT) and lysosomal exopeptidases (dipeptidyl peptidase I (DPP I), dipeptidyl peptidase II (DPP II) was investigated in rabbit, ox and pig corneas. Cryostat sections of snap-frozen corneas treated with chloroform-acetone (4°C) were used for the demonstration of membrane-bound enzymes and sections of corneas fixed in 4% paraformaldehyde (4°C) for the demonstration of lysosomal enzymes.In activities of proteases species differences were found. The rabbit cornea was most active, followed by ox and pig corneas. Individual corneal layers reacted differently. Of membrane proteases a high APM activity was found in keratocytes, whereas epithelium and endothelium were negative. On the other hand APA and GGT were active in the epithelium and endothelium. Their activities in keratocytes were less pronounced. DPP IV activity was demonstrated in some keratocytes beneath the epithelium only. Lysosomal enzymes DPP I and DPP II were active in all corneal layers. The epithelium displayed the highest activity.Differences in activities in the centro-peripheral and epithelio-endothelial directions were found. DPP I, DPP II, and APM were most active in the limbal region in all corneal layers.  相似文献   

3.
The lymphocytes of the rat thymus can be grossly differentiated by their cell membrane-bound proteinases. Subcapsular thymocytes lack aminopeptidase A (APA) and AMP and gamma-glutamyltranspeptidase (GGT). Cortical thymocytes show a high activity of APA but no APM and no GGT. Medullar thymocytes possess a high GGT and APM activity but are free of APA. Under Mg deficiency, the APA-negative subcapsular thymocytes are reduced. In lymphoma and beginning lymphoma, APA, APM and GGT are absent. In lymphoma, the alkaline phosphatase activity is increased. Differences are found for dipeptidylpeptidase IV (DPP IV). In some lymphoma, its activity is reduced, in others the DPP IV activity is increased.  相似文献   

4.
Histochemistry of some proteases in the normal rabbit, pig and ox corneas   总被引:1,自引:0,他引:1  
The distribution of activities of membrane aminopeptidases (aminopeptidase M (APM), aminopeptidase A (APA), dipeptidyl peptidase IV (DPP IV), gamma-glutamyltransferase (GGT) and lysosomal exopeptidases (dipeptidyl peptidase I (DPP I), dipeptidyl peptidase II (DPP II)) was investigated in rabbit, ox and pig corneas. Cryostat sections of snap-frozen corneas treated with chloroform-acetone (4 degrees C) were used for the demonstration of membrane-bound enzymes and sections of corneas fixed in 4% paraformaldehyde (4 degrees C) for the demonstration of lysosomal enzymes. In activities of proteases species differences were found. The rabbit cornea was most active, followed by ox and pig corneas. Individual corneal layers reacted differently. Of membrane proteases a high APM activity was found in keratocytes, whereas epithelium and endothelium were negative. On the other hand, APA and GGT were active in the epithelium and endothelium. Their activities in keratocytes were less pronounced. DPP IV activity was demonstrated in some keratocytes beneath the epithelium only. Lysosomal enzymes DPP I and DPP II were active in all corneal layers. The epithelium displayed the highest activity. Differences in activities in the centro-peripheral and epithelio-endothelial directions were found. DPP I, DPP II, and APM were most active in the limbal region in all corneal layers.  相似文献   

5.
Summary In a previous paper, combined dye histochemistry and analytical isoelectric focusing (IEF) of supernatants from organ homogenates have been shown to yield good results for the detection of protease isoenzymes. Difficulties arise when the protease to be studied is partially or completely inhibited y diazonium salts and when synthetic peptide substrates different from 4-methoxy-2-naphthylamine (MNA) amino acids and peptides are to be used. In this paper a technique is described in which cellulose acetate foils impregnated with MNA, 7-amino-4-methylcoumarin (AMC) and 7-amino-4-trifluoromethylcoumarin (AFC) substrates are overlaid on electrophoresis strips after IEF. After incubation, the foils are viewed with an UV-lamp and photographed. The MNA, AMC and AFC peptides are equally suitable for fluorescence band detection. Using this technique, occasionally protease isoenzymes are found which are more sensitive towards diazonium salts, e.g. aminopeptidase A and M. Sometimes it is also possible to detect thiolproteases which is not the case when employing dye histochemistry.  相似文献   

6.
Summary Aminopeptidase M (APM), aminopeptidase A (APA), dipeptidyl peptidase IV (DPP IV) and -glutamyl transferase (GGT) were demonstrated histochemically in cryostat sections of the rat brain to show the reaction pattern of ependyma, choroid plexus and leptomeninges. GGT was only demonstrable in the cell membranes of ependymal cells and in the leptomeninges; however, APA, APM and DAP IV showed a variable degree of activity in the capillary endothelium of the choroid plexus as well as in the leptomeninges. On the basis of these results, it is postulated that peptides in the cerebrospinal fluid can be cleaved extraventricularly by the enzymes demonstrated in the leptomeninges.Dedicated to Professor Dr. T.H. Schiebler on the occasion of his 65th birthday  相似文献   

7.
Histochemistry of proteases in ependyma, choroid plexus and leptomeninges   总被引:1,自引:0,他引:1  
A Mitro  Z Lojda 《Histochemistry》1988,88(3-6):645-646
Aminopeptidase M (APM), aminopeptidase A (APA), dipeptidyl peptidase IV (DPP IV) and gamma-glutamyl transferase (GGT) were demonstrated histochemically in cryostat sections of the rat brain to show the reaction pattern of ependyma, choroid plexus and leptomeninges. GGT was only demonstrable in the cell membranes of ependymal cells and in the leptomeninges; however, APA, APM and DAP IV showed a variable degree of activity in the capillary endothelium of the choroid plexus as well as in the leptomeninges. On the basis of these results, it is postulated that peptides in the cerebrospinal fluid can be cleaved extraventricularly by the enzymes demonstrated in the leptomeninges.  相似文献   

8.
In the thymus of normally fed pregnant rats the plasma membrane enzymes dipeptidyl peptidase IV (DPP IV) and alkaline phosphatase (alP) were found in cortical and medullary lymphocytes (thymocytes). Plasma membrane aminopeptidase A (APA) and adenosine monophosphate hydrolysing phosphatase (AMPP) were present in cortical reticular cells. In medullary reticular cells, aminopeptidase M (APM), gamma-glutamyl transferase (GGT), adenosine triphosphate (ATPP) and thiamine pyrophosphate (TPPP) cleaving phosphatases were detected. Medullary reticular cells did not contain APA. Lysosomal DPP I and II, acid phosphatase, acid beta-D-galactosidase, beta-D-N-acetyl-glucosaminidase, beta-D-glucuronidase and non-specific esterases occurred especially in macrophages at the corticomedullary junction. The 21-day-old fetal thymus showed a similar reaction pattern as the maternal organ except for APA which was absent before birth. After treatment of the pregnant rats with valproic acid (VPA), salicylic acid (SA), streptozotocin (ST) and retinoic acid (RA) APA showed an increase in activity in the thymic cortex. In addition, ST and RA induced AMPP, ATPP and TPPP activity in cortical reticular cells up to the same pattern as in medullary reticular cells. After ethanol (ET) administration severe damages occurred. The thymic cortex was free of DPP IV-positive lymphocytes; the medullary reticular cells showed reduced or no GGT and occasionally an increased APM activity. Dexamethasone (DEXA) given to normal or zinc-deficient rats produced the most severe lesions; thymocytes with DPP IV activity were completely absent in the cortex and medulla. In Zn-deficient pregnant rats similar alterations were observed as after ET.(ABSTRACT TRUNCATED AT 250 WORDS)  相似文献   

9.
R Gossrau 《Histochemistry》1979,60(2):231-248
Fresh frozen, unfixed, chloroforme-acetone treated or freeze-dried cryostat sections or sections from aldehyde-fixed blocks of tissue were tried for the histochemical investigation of dipeptidylpeptidase IV (DPP IV) with L-glycyl-L-prolyl(gly-pro)-naphthylamides as substrates and stable or unstable diazonium salts for simultaneous coupling and various buffers, pH 5--7.5 in rats, mice, guinea-pigs, cats, rabbits, hamsters and human enterobiopsies. The best results are obtained with 1.7--3.4 mM gly-pro-4-methoxy-2-naphthylamide and 1 mg Fast Blue B/ml or (with some limitations) 0.025 ml hexazotized new fuchsine/ml in 0.1 M cacodylate or phosphate buffer, pH 7.5 and unfixed sections for the demonstration of the total activity of DPP IV and freeze-dried celloidin-mounted cryostat sections for the precise localization of the enzyme or the detection of lysosomes, Golgi apparatus and secretion granules sections from aldehyde fixed tissue blocks are only suitable to study the lysosomal hydrolysis of gly-pro-naphthylamides between pH 5 and 7 when hexazotized p-rosaniline or new fuchsine are employed. DPP IV is firmly bound to strutures and shows species- and organ-dependent differences. In general, the enzyme occurs in the capillary endothelium, sinusoidal cells, perineurium, epithelial cells of intercalated and striated ducts, microvillous zone of intestinal crypts and villi, uterus, Fallopian tubes, ductus epididymis and proximal renal tubules, hepatocyte and lymphocyte membrane, plasmalemma of pseudostratified and transient epithelia and in the capsules and interstitium of many organs. These sites of activity can be completely inhibited by diisopropyl fluorophosphate and partially by Pb2+; Mg2+, Mn2+, Co2+ EDTA are without any influence. Phenantrolin may activate DPP IV. The biochemical assay works with 10 mM gly-pro-2-naphthylamide in 0.1 M cacodylate buffer, pH 7; the enzyme activity is determined fluorometrically in guinea-pig and rat organs; the data confirm and enlarge the species- and organ-dependent differences revealed by histochemistry. Compared with other dipeptide as well as tripeptide and amino acid naphthylamides the results obtained for DPP IV suggest a peptidylpeptidase which seems to be involved in other metabolic processes beside the degradation of collagen.  相似文献   

10.
Summary In the thymus of normally fed pregnant rats the plasma membrane enzymes dipeptidyl peptidase IV (DPP IV) and alkaline phosphatase (alP) were found in cortical and medullary lymphocytes (thymocytes). Plasma membrane aminopeptidase A (APA) and adenosine monophosphate hydrolysing phosphatase (AMPP) were present in cortical reticular cells. In medullary reticular cells, aminopeptidase M (APM), -glutamyl transferase (GGT), adenosine triphosphate (ATPP) and thiamine pyrophosphate (TPPP) cleaving phosphatases were detected. Medullary reticular cells did not contain APA. Lysosomal DPP I and II, acid phosphatase, acid -d-galactosidase, -d-N-acetylglucosaminidase, -d-glucuronidase and non-specific esterases occurred especially in macrophages at the corticomedullary junction. The 21-day-old fetal thymus showed a similar reaction pattern as the maternal organ except for APA which was absent before birth.—After treatment of the pregnant rats with valproic acid (VPA), salicylic acid (SA), streptozotocin (ST) and retinoic acid (RA) APA showed an increase in activity in the thymic cortex. In addition, ST and RA induced AMPP, ATPP and TPPP activity in cortical reticular cells up to the same pattern as in medullary reticular cells. After ethanol (ET) administration severe damages occurred. The thymic cortex was free of DPP IV-positive lymphocytes; the medullary reticular cells showed reduced or no GGT and occasionally an increased APM activity. Dexamethasone (DEXA) given to normal or zinc-deficient rats produced the most severe lesions; thymocytes with DPP IV activity were completely absent in the cortex and medulla. In Zn-deficient pregnant rats similar alterations were observed as after ET. When the drugs were applied to Zn-deficient pregnant rats, the alterations resembled those observed after drug treatment alone. In all cases of severe thymus degeneration, i.e. ET and DEXA treatment and Zn-deficiency, the number of macrophages and activities of lysosomal hydrolases in macrophages and reticular cells were increased; the lysosomal hydrolases were often homogeneously distributed over the cortex. Cell contacts between reticular cells and lymphocytes were reduced. Vacuoles occurred within the reticular cells.—The fetal thymus was reduced in size and the number of macrophages and the activities of their lysosomal enzymes were increased after Zn-deficiency, DEXA treatment and Zn-deficiency combined with ET administration.Supported by the Deutsche Forschungsgemeinschaft (Sfb 174)  相似文献   

11.
Synopsis The numerous osteoclasts in a giant cell tumour of bone were found to possess at least two distinct phosphatases capable of hydrolysing naphthol AS-TR phosphate. An acid phosphatase, with optimum activity about pH 4.7, could be demonstrated by simultaneous coupling with Fast Bordeaux OL or Red Violet LB, but not with Fast Red TR. The last-named salt, on the other hand, could be used for demonstrating a phosphatase with an optimum pH of activity about 7.3, showing some activity as an alkaline phosphatase at pH 8.3. This enzyme was markedly inhibited by zinc ions and could not be demonstrated by simultaneous coupling with diazonium salts stabilized with zinc chloride. The acid phosphatase was much less sensitive to zinc, but showed marked inhibition by aluminium, which had comparatively little effect on the other enzyme. Some discrepancies between the published formulae of stable diazonium salts and the substances found to be present in them are discussed.  相似文献   

12.
R Gossrau 《Histochemistry》1978,57(4):323-342
Using fresh frozen, freeze-dried or cryostate sections from aldehyde fixed rat tissues 13 diazonium salts were tested as simultaneous coupling reagents for the localization of acid, neutral and alkaline hydrolases with azo indoxyl methods. Hexazotized new fuchsine and/or Fast blue B are the diazonium salts of choice for the demonstration of acid beta-galactosidase, neuraminidase, beta-N-acetylglucosaminidase, acid phosphatase, and non-specific esterase followed by hexazotized p-rosaniline. Fast blue VB, BB and RR and Fast violet B are recommended for the investigation of alkaline phosphatase and lactase, Fast garnet GBC for acid beta-galactosidase, glucosaminidase and lactase. Fast red B, RC, RL and TR and Fast black K can only be employed for lactase studies. The exact concentration of the coupling reagent depends on the activity of the enzyme and the organ imvestigated. On the average 0.01-0.02 ml unstable diazonium salt/ml and 0.3--1 microgram stable diazonium salt/ml are sufficient for the correct localization of these hydrolases. Freeze-dried cryostat sections yield the best results in the demonstration of lactase and alkaline phosphatase independent on the coupling reagent used. Sections from formaldehyde or glutaraldehyde fixed organs are superior for the localization of the other hydrolases; an exception is the investigation of acid beta-galactosidase and glucosaminidase with Fast garnet GBC. Then, excellent results are obtained also with freeze-dried material. Fresh frozen sections are suitable for the localization of lactase with hexazotized new fuchsine or p-rosaniline and of alkaline phosphatase with Fast blue VB and BB or violet B. The total activity of acid, neutral and alkaline hydrolases can be investigated using semipermeable membranes in combination with all unstable and stable diazonium salts of choice. Reliable osmification of the azoindoxyl dye is only possible if hexazotized p-rosaniline is employed for coupling; without further posttreatment all azoindoxyl dyes are extracted by ethanol, isopropanol or xylol. 7 incubation media are given for the demonstration of hydrolases with azoindoxyl methods at the level of light microscopy for routine studies and typical examples for the application of these methods are presented. A modified procedure is described for the freeze-drying of cryostat sections with the Edwards-Pearse tissue dryer EPD3.  相似文献   

13.
A quantitative histochemical study of dipeptidylpeptidase IV (DPP IV)   总被引:2,自引:0,他引:2  
Summary In order to elucidate the possibility of a quantitative study of dipeptidylpeptidase IV (DPP IV) in cells and cell compartments of tissue sections kinetic investigations were performed with biochemical fluorometric and cytophotometric (microdensitometric) methods in the jejunum, kidney and liver of adult rats; in addition, two approaches of microdensitometric measuring (endpoint and continuous cytophotometry) were compared. Biochemically, Gly-Pro-4-methoxy-2-naphthylamine (MNA) is the best substrate compared with the 1-naphthylamine and 2-naphthylamine due to its high hydrolysis rate, the low Michaelis constant (Km) and the relative high fluorescence of MNA. Its pH optimum is between 8.5 and 9. The hydrolysis rates delivered by cacodylate, phosphate and Tris HCl are similar and always higher than with other buffers. The maximal reaction velocity is reached with 3 mM Gly-Pro-MNA. The hydrolysis is inhibited in the presence of phenantroline, diisopronyl fluorphosphate, formaldehyde and diazonium salts; furthermore, formaldehyde and diazonium salts increase the Km of DPP IV. Fast Blue B pure (FBB) is the simultaneous coupling reagent of choice. End-point (plug and scanning procedure) and continuous microdensitometry with Gly-Pro-MNA and FBB in the intestinal and renal brush border and in renal glomerula have to be carried out at suboptimal pH (7.5). However, the optimal substrate concentrations are identical and the overall relation between the activity of DPP IV in the jenum, liver and kidney are similar in the quantitative histochemical and biochemical system. A linear relationship between the quantity of azo-dye and section thickness or incubation time exists between 4 m and 10 m and during the first 6 min of incubation respectively. Among different plotting procedures the best-fit method delivers the most reliable results. — The microdensitometric data in the small intestine show that Km and Vmax differ at different positions of the villi and may represent parameters for the maturation process of the enterocytes; in the kidney microdensitometry reveals different DPP IV activities in the different parts of the nephron. Both, the findings for the villi and the nephron cannot be obtained by biochemical methods.Supported by Deutsche Forschungsgemeinschaft (GU 184/1)Supported in part by Deutsche Forschungsgemeinschaft (SFB 105)  相似文献   

14.
Zusammenfassung An frischen, gefriergetrockneten und Schnitten von aldehyd-fixierten Rattengeweben werden 13 Diazoniumsalze als Simultankuppler zum Nachweis saurer, neutraler und alkalischer Hydrolasen mit Azoindoxylverfahren geprüft. Hexazotiertes Neufuchsin und/oder Fast Blue B sind die Diazoniumsalze der Wahl zur Lokalisation von saurer -Galactosidase, Neuraminidase, -N-Acetylglucosaminidase, saurer Phosphatase und unspezifischer Esterase gefolgt von Hexazonium-p-rosanilin. Fast Blue VB, BB und RR sowie Fast Violet B eignen sich zur Untersuchung von Lactase und alkalischer Phosphatase; Fast Garnet GBC kann zur Lokalisation von saurer -Galactosidase, Glucosaminidase und Lactase, Fast Red B, RC, RL und TR sowie Black K nur für Lactase-Studien verwandt werden. Durchschnittlich reichen 0,01–0,02 ml instabiles Diazoniumsalz und 0,3–1 mg stabiles Diazoniumsalz/ml zur korrekten Lokalisation dieser Hydrolasen aus. Im einzelnen hängt die Kupplerkonzentration von der Enzymaktivität und vom untersuchten Organ ab. Gefriergetrocknete Kryostatschnitte liefern unabhängig vom Kuppler die besten Resultate bei Untersuchung von Lactase und alkalischer Phosphatase; Schnitte von form- oder glutaraldehyd-fixierten Organen sind beim Nachweis der restlichen Hydrolasen überlegen. Eine Ausnahme macht die Untersuchung der sauren -Galactosidase und Glucosaminidase mit Fast Garnet GBC; dann werden die besten Ergebnisse nach Gefriertrocknung erzielt.Frische Kryostatschnitte sind zur Darstellung der Lactase mit hexazotiertem Neufuchsin oder p-Rosanilin und der alkalischen Phosphatase mit Fast Blue VB und BB sowie Violet B geeignet; die Gesamtaktivität der sauren, neutralen und alkalischen Hydrolasen kann mit semipermeablen Membranen und den stabilen sowie instabilen Diazoniumsalzen der Wahl untersucht werden.Ausreichende Osmierung der Azoindoxylfarbstoffe ist nur möglich, wenn Hexazonium-p-rosanilin als Kupplungsreagens benutzt wird; ohne Vorbehandlung extrahieren Äthanol, Isopropanol und Xylol alle Azoindoxyle.7 Inkubationsmedien werden zum lichtmikroskopisch-histochemischen Nachweis von Glykosidasen, Esterasen und Phosphatasen mit Azoindoxylmethoden angegeben und typische Anwendungsbeispiele genannt. Zur Gefriertrocknung von Kryostatschnitten mit dem Edwards-Pearse Gewebetrockner EPD 3 wird ein modifiziertes Verfahren beschrieben.
Azoindoxyl methods for the investigation of hydrolasesIV. Suitability of various diazonium salts
Summary Using fresh frozen, freeze-dried or cryostate sections from aldehyde fixed rat tissues 13 diazonium salts were tested as simultaneous coupling reagents for the localization of acid, neutral and alkaline hydrolases with azo indoxyl methods. Hexazotized new fuchsine and/or Fast blue B are the diazonium salts of choice for the demonstration of acid -galactosidase, neuraminidase, -N-acetylglucosaminidase, acid phosphatase, and non-specific esterase followed by hexazotized p-rosaniline. Fast blue VB, BB and RR and Fast violet B are recommended for the investigation of alkaline phosphatase and lactase, Fast garnet GBC for acid -galactosidase, glucosaminidase and lactase. Fast red B, RC, RL and TR and Fast black K can only be employed for lactase studies. The exact concentration of the coupling reagent depends on the activity of the enzyme and the organ investigated. On the average 0.01–0.02 ml unstable diazonium salt/ml and 0.3–1 mg stable diazonium salt/ml are sufficient for the correct localization of these hydrolases. Freeze-dried cryostat sections yield the best results in the demonstration of lactase and alkaline phosphatase independent on the coupling reagent used. Sections from formaldehyde or glutaraldehyde fixed organs are superior for the localization of the other hydrolases; an exception is the investigation of acid -galactosidase and glucosaminidase with Fast garnet GBC. Then, excellent results are obtained also with freeze-dried material.Fresh frozen sections are suitable for the localization of lactase with hexazotized new fuchsine or p-rosaniline and of alkaline phosphatase with Fast blue VB and BB or violet B. The total activity of acid, neutral and alkaline hydrolases can be investigated using semipermeable membranes in combination with all unstable and stable diazonium salts of choice.Reliable osmification of the azoindoxyl dye is only possible if hexazotized p-rosaniline is employed for coupling; without further posttreatment all azoindoxyl dyes are extracted by ethanol, isopropanol or xylol.7 incubation media are given for the demonstration of hydrolases with azoindoxyl methods at the level of light microscopy for routine studies and typical examples for the application of these methods are presented. A modified procedure is described for the freeze-drying of cryostat sections with the Edwards-Pearse tissue dryer EPD 3.


Mit Unterstützung durch die Deutsche Forschungsgemeinschaft (SFB 105)  相似文献   

15.
The suitability of Z-Arg-Gly-Phe-Phe-Leu-MNA and Z-Arg-Gly-Phe-Phe-Pro-MNA for the assessment of cathepsin D activity was tested in biochemical and histochemical experiments. Substrates were dissolved in dimethylformamide and used at 0.1-0.5 mM in various buffers over a pH range of 3.5-7.4. Homogenates of various rat organs and isolated purified enzymes [cathepsin D from bovine spleen, dipeptidyl peptidase (DPP) IV from porcine kidney and rat lung] were used as enzyme sources. Pepstatin, di-isopropylfluorophosphate (DFP), p-chloromercuribenzoate, o-phenanthroline and a series of DPP IV inhibitors were used in inhibitor experiments. At pH 3.5 and 5.0, substrates were used in a two-step postcoupling procedure with aminopeptidase M and dipeptidyl peptidase IV as auxiliary enzymes and Fast Blue BB as coupling agent. Results were compared with those obtained with haemoglobin. Above pH 5.0 substrates were used in a one-step postcoupling procedure. Cryostat sections of snap-frozen or cold aldehyde-fixed tissue pieces of various rat organs and biopsies of human jejunal mucosa were used in histochemical experiments. As in biochemical tests a two-step procedure was used in the pH range 3.5-5.0, but Fast Blue B was used in the second step for the simultaneous coupling. Above pH 5.0 a one-step simultaneous azo coupling procedure was used with Fast Blue B as coupling agent. At pH 3.5 the hydrolysis rate of both synthetic substrates was about 100x lower than that of haemoglobin when cathepsin D from bovine spleen was used.(ABSTRACT TRUNCATED AT 250 WORDS)  相似文献   

16.
In this study, we determined the activities of four aminopeptidases such as aminopeptidase B (APB), M (APM), N (APN) and dipeptidylpeptidase IV (DPP IV) in Caco-2 cells and compared with those in the rat intestinal mucosae. The activities of APB, APM and APN appeared to be highest in rat small intestinal mucosa, while DPP IV activity was much higher in Caco-2 cells than that in the rat intestinal mucosa. Next the inhibitory effects of various protease inhibitors were examined in Caco-2 homogenate. Three tested inhibitors, bacitracin, amastatin and puromycin, effectively inhibited the activities of APM, APN and DPP IV except for APB. Further, we quantitatively evaluated the permeation and degradation properties of leucine enkephalin (Leu-Enk) in the presence or absence of inhibitors in Caco-2 monolayer system. Leu-Enk had a high degradation clearance (CLd) and a low permeation clearance (CLp) in Caco-2 monolayers. This finding indicates that the very rapid degradation of Leu-Enk on the apical side of Caco-2 monolayers was due to aminopeptidases. However, these protease inhibitors besides sodium glycocholate were able to reduce the CLd values markedly, thereby increasing the permeation amount of Leu-Enk across Caco-2 monolayers. In particular, amastatin significantly decreased the CLd value and increased the CLp value. This enhanced CLp value was further increased by the coadministration with an absorption enhancer, EDTA or laurylmaltoside. These findings are relevant to the oral administration of peptide drugs and to developing an efficient oral delivery system.  相似文献   

17.
Summary Quantitative histochemical measurements of aminopeptidase A (APA; E.C.3.4.11.7) were done kinetically in the kidney glomeruli of rat and mouse with an instrumental setup consisting of a microdensitometer and a computer-supported morphometric system. The histochemical demonstration of APA was carried out using the simultaneous azo coupling technique (purest-grade Fast Blue B as coupling agent and -l-glutamic acid-4-methoxy-2-naphthylamide as substrate). The methodological studies show that APA activity is calcium-ion-dependent and increases linearly with the thickness of the tissue section (3–12 m) and that the time-course of APA activity as determined by linear regression is linear only for the first 1 to 2 min of the reaction. — Kinetic measurements indicate a 40% decrease in APA activities when -l-glutamic acid-4-methoxy-2-naphthylamide (-l-Glu-MNA) is replaced by -l-aspartic acid-4-methoxy-2-naphthylamide. When -l-Glu-MNA is replaced with l-alanine-4-methoxy-2-naphthylamide, which is a substrate of aminopeptidase M (APM) only very low reaction rates are measurable (about 1.4% of those with -l-Glu-MNA). 100 and 130 mM NaCl in the incubation medium increase APA activities by approximately 16%–17%. — To clarify the functional importance of APA in the kidney, their activities were measured under the influence of angiotensins. The glomerulus was selected as the measuring site, for besides APA it contains no APM or other peptidases that could degrade angiotensins (the glomerular dipeptidyl peptidase IV is not inhibited by angiotensin II). Using the Lineweaver-Burk plot, we determined a K m of 0.16 mM for the APA in rat glomeruli and 0.14 mM in mouse glomeruli. The V max in mouse glomeruli is 1.6 times higher than in rat glomeruli. Ang iotensin I, II and III competitively inhibit APA in the rat and mouse glomeruli. — With quantitative histochemical techniques it was possible to show that APA is equivalent to angiotensinase A (splitting off the N-terminal aspartic acid from angiotensin I and II).Supported by the Deutsche Forschungsgemeinschaft (SFB 105)  相似文献   

18.
Summary The usefulness of the analytical electrofocusing in a thin-layer polyacrylamide (PAG) plate is shown on the basis of experiments with 10%–20% homogenates of various rat, rabbit and human organs as well as in lysates of isolated human lymphocytes and leucocytes in 2% Triton X100. 0.1–0.3 l of 12000 g supernatants were applied on LKB Ampholine PAG plates pH range 3.5–9.5 and subjected to electrofocusing. Afterwards portions of PAG plates were processed in optimized histochemical media for the demonstration of enzymes cleaving peptide bonds using various substrates. The same media were used in the histochemical detection of enzymes in sections on slides or semipermeable membranes. Electrofocused zymograms display species and organ differences. Ala-MNA, Leu-MNA and Met-MNA furnish similar zymograms. Bands obtained with Ala-MNA are most intense. Zymograms with Gly-Pro-MNA and Lys-Pro-MNA at pH 7.2 are not entirely identical. The majority of bands is more intense when Gly-Pro-MNA is used as the substrate and is due to the activity of DAP IV. The anodal band(s) focusing around pH 4.9 (rat) or 5.5 (man) is (are) much stronger with Lys-Pro-MNA and DAP II is responsible for it (them). Zymograms with His-Ser-MNA and Lys-Ser-MNA are similar. However, they differ form those revealed with Gly-Pro-MNA and Lys-Pro-MNA. Zymograms of lysates of leucocytes obtained with naphthol AS-D-chloroacetate and Ac-Ala-l-naphthyl ester are not identical showing that more than one enzyme is responsible for the bands. Results obtained with closely related substrates such as Ac-Ala-l-naphthyl ester and Ac-Met-l-naphtyl ester are not identical either. Zymograms of lysates of human lymphocytes revealed with Gly-Pro-MNA at pH 7.2 and Lys-Ala-MNA or Lys-Pro-MNA at pH 5.5 or 5.3 respectively show clearly the presence of DAP IV and DAP II in these cells. The analytical electrofocusing in PAG plates is a very useful tool in the histochemistry (and biochemistry) of enzymes cleaving peptide bonds. It helps very much in the evaluation of the substrate specificity, choosing of the discriminating substrate and enables a quick and reliable testing of the quality of various batches of commercially supplied substrates, diazonium salts and other reagents. The correlation of zymograms with the in situ pattern helps in the elucidation of the origin of individual bands in zymograms and suggests different molecular forms of peptidases in different localizations.  相似文献   

19.
Zusammenfassung Histochemisch wird die Dipeptidylpeptidase IV (DPP IV) mit Glycyl-prolyl(Gly-pro)-naphthylamiden als Substraten, stabilen und instabilen Diazoniumsalzen zur Simultankupplung und unterschiedlichen Puffern bei Ratten, Mäusen, Katzen, Meerschweinchen, Kaninchen, Hamstern und in menschlichen Dünndarmbiopsien nach verschiedenen Gewebevorbehandlungen untersucht. Die besten Resultate liefert 1,7–3,4 mM Gly-pro-4-methoxy-2-naphthylamid und 1 mg Fast Blue B/ml und mit Einschränkungen 0,025 ml hexazotiertes Neufuchsin/ml in 0,1 M Cacodylat- oder Phosphat-Puffer, pH 7,5, und frische Kryostatschnitte zum Nachweis der Gesamtaktivität der DPP IV und gefriergetrocknete Schnitte nach Celloidinmontage zur ortsgetreuen Lokalization des Enzyms. Schnitte von aldehydfixiertem Material eignen sich zur Untersuchung des Umsatzes von Gly-pro-naphthylamiden zwischen pH 5 und 7 mit hexazotiertem Neufuchsin oder p-Rosanilin in Lysosomen.Die DPP IV ist fest strukturgebunden und weist Spezies- und Organdifferenzen auf. Im allgemeinen kommt das Enzym in Kapillarendothelien, Sinusoidalzellen, Perineurium, Schalt- und Sekretrohrepithelien, Mikrovillizone von Darmkrypten und-zotten, Uterus, Tube, proximalen Nierentubuli sowie Nebenhodengang, Hepatocyten- und Lymphocytenmembran, Plasmalemm mehrschichtiger und Übergangsepithelien sowie in der Kapsel und im Interstitium zahlreicher Organe vor.Die biochemische Untersuchung der DPP IV wird mit 10 mM Gly-pro-2-naphthylamid in 0.1 M Cacodylat-Puffer, pH 7 durchgeführt und die Enzymaktivität fluorometrisch in Ratten- und Meerschweinchenorganen bestimmt. Die Befunde bestätigen und erweitern die auffälligen spezies- und organabhängigen Unterschiede des histochemischen DPP IV-Nachweises.Verglichen mit anderen Di- sowie Tripeptidyl- und Aminosäurenaphthylamiden deuten die Befunde darauf hin, daß es sich bei der DPP IV um eine Peptidylpeptidase handelt, die neben dem Kollagenabbau an anderen Stoffwechselvorgängen beteiligt ist.
Histochemical and biochemical distribution of dipeptidylpeptidase IV (DPP IV)
Summary Fresh frozen, unfixed, chloroforme-acetone treated or freeze-dried cryostat sections or sections from aldehyde-fixed blocks of tissue were tried for the histochemical investigation of dipeptidylpeptidase IV (DPP IV) with l-glycyl-l-prolyl(gly-pro)-naphthylamides as substrates and stable or unstable diazonium salts for simultaneous coupling and various buffers, pH 5–7.5 in rats, mice, guinea-pigs, cats, rabbits, hamsters and human enterobiopsies. The best results are obtained with 1.7–3.4 mM gly-pro-4-methoxy-2-naphthylamide and 1 mg Fast Blue B/ml or (with some limitations) 0.025 ml hexazotized new fuchsine/ml in 0.1 M cacodylate or phosphate buffer, pH 7.5 and unfixed sections for the demonstration of the total activity of DPP IV and freeze-dried celloidin-mounted cryostat sections for the precise localization of the enzyme or the detection of lysosomes, Golgi apparatus and secretion granules; sections from aldehyde fixed tissue blocks are only suitable to study the lysosomal hydrolysis of gly-pro-naphthylamides between pH 5 and 7 when hexazotized p-rosaniline or new fuchsine are employed.DPP IV is firmly bound to structures and shows species- and organ-dependent differences. In general, the enzyme occurs in the capillary endothelium, sinusoidal cells, perineurium, epithelial cells of intercalated and striated ducts, microvillous zone of intestinal crypts and villi, uterus, Fallopian tube, ductus epididymis and proximal renal tubules, hepatocyte and lymphocyte membrane, plasmalemma of pseudostratified and transient epithelia and in the capsules and interstitium of many organs. These sites of activity can be completely inhibited by diisopropyl fluorophosphate and partially by Pb2+; Mg2+, Mn2+, Co2+ EDTA are without any influence. Phenantrolin may activate DPP IV.The biochemical assay works with 10 mM gly-pro-2-naphthylamide in 0.1 M cacodylate buffer, pH 7; the enzyme activity is determined fluorometrically in guinea-pig and rat organs; the data confirm and enlarge the species-and organ-dependent differences revealed by histochemistry.Compared with other dipeptide as well as tripeptide and amino acid naphthylamides the results obtained for DPP IV suggest a peptidylpeptidase which seems to be involved in other metabolic processes beside the degradation of collagen.


Mit Unterstützung durch die Deutsche Forschungsgemeinschaft (SFB 105)  相似文献   

20.
Summary The suitability of Z-Arg-Gly-Phe-Phe-Leu-MNA and Z-Arg-Gly-Phe-Phe-Pro-MNA for the assessment of cathepsin D activity was tested in biochemical and histochemical experiments. Substrates were dissolved in dimethylformamide and used at 0.1–0.5 mM in various buffers over a pH range of 3.5–7.4. Homogenates of various rat organs and isolated purified enzymes [cathepsin D from bovine spleen, dipeptidyl peptidase (DPP) I.V from porcine kidney and rat lung] were used as enzyme sources. Pepstatin, di-isopropylfluorophosphate (DFP),p-chloromercuribenzoate,o-phenanthroline and a series of DPP IV inhibitors were used in inhibitor experiments. At pH 3.5 and 5.0, substrates were used in a two-step postcoupling procedure with aminopeptidase M and dipeptidyl peptidase IV as auxiliary enzymes and Fast Blue BB as coupling agent. Results were compared with those obtained with haemoglobin. Above pH 5.0 substrates were used in a one-step postcoupling procedure.Cryostat sections of snap-frozen or cold aldehyde-fixed tissue pieces of various rat organs and biopsies of human jejunal mucosa were used in histochemical experiments. As in biochemical tests a two-step procedure was used in the pH range 3.5–5.0, but Fast Blue B was used in the second step for the simultancous coupling. Above pH 5.0 a onestep simultaneous azo coupling procedure was used with Fast Blue B as coupling agent.At pH 3.5 the hydrolysis rate of both synthetic substrates was about 100 x lower than that of haemoglobin when cathepsin D from bovine spleen was used. The activity was inhibited by pepstatin. With increasing pH the hydrolysis rate of Z-Arg-Gly-Phe-Phe-Pro-MNA increased, while that of Z-Arg-Gly-Phe-Phe-Leu-MNA decreased when organ homogenates were used as enzyme sources. However, the activity was not inhibited by pepstatin. It was inhibited by DFP. The extent of the inhibition with other substances was species and organ dependent. Z-Arg-Gly-Phe-Phe-Pro-MNA was also cleaved by isolated and purified DPP IV of porcine kidney and rat lung and the activity was inhibited by DFP and DPP IV inhibitors.In histochemical experiments the staining obtained with both synthetic substrates at pH 3.5 was weak and rather diffuse, with only slight accentuation or none at all in the lysosomal region of cells. In the pH range 5.5–7.4 a very distinct reaction was observed with Z-Arg-Gly-Phe-Phe-Pro-MNA only. The reaction product was localized in the brush border of enterocytes and of cells of the proximal kidney tubules. Endothelial cells of glomeruli and capillaries of the propria of the human jejunum also displayed a positive reaction. Lymphocytes in the propria of rat small intestine reacted to some extent. The reaction was inhibited by DFP. The extent of the inhibition with other substances varied.Z-Arg-Gly-Phe-Phe-Leu-MNA and Z-Arg-Gly-Phe-Phe-Pro-MNA are not efficient substrates for the assessment of cathepsin D activity. In histochemical studies diffusion artifacts must always be considered. In the pH range 5.5–7.4, Z-Arg-Gly-Phe-Phe-Pro-MNA is cleaved by a serine endopeptidase and by a metalloendopeptidase. It remains to be established whether prolyl endopeptidase or DPP IV (or both) and which metalloendopeptidase are responsible for the cleavage. In the evaluation of enterobiopsies the demonstration of this activity is a sensitive means for the assessment of the state of the brush border.Dedicated to Professor Dr. T.H. Schiebler on the occasion of his 65th birthday.  相似文献   

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