Auxin-induced delay of abscission: The involvement of calcium ions and protein phosphorylation in bean explants

Treatment with Ca²⁺ channel blockers such as lanthanum chloride and verapamil promoted abscission in pulvinar explants of bean ( Phaseolus vulgaris L. ev. Pirate). In addition, auxin-induced delay of abscission was markedly reduced in the presence of Ca²⁺ channel blockers. In vitro phosphorylation studies were performed using membrane preparations (130000 g pellet) from freshly excised as well as auxintreated and control (minus auxin) pulvinar sections. Auxin-treated sections showed a 66 kDa phosphoprotein as well as Ca²⁺ -dependent phosphorylation that were not observed in control explants.
Coomassie blue stammg of soluble proteins (130000 g supernatent) separated on SDS-PAGE revealed the presence of 62. 55 and 47 kDa polypeptides only in the freshly excised pulvini. However. no distinct changes were observed in soluble protein profile between auxin-treated and control explants. When soluble proteins were phosphorylated in vitro, Ca²⁺ promoted the phosphorylation of 92, 55. 40 and I7 kDa polypeptides only in freshly excised pulvmi. Ca²⁺-dependent phosphorylation of soluble proteins was not observed in either the control or auxin-treated explants. In addition. in vivo phosphorylation studies were performed using freshly excised. auxrn-treated and control explants. Freshly excused segments and auxin-treated ex-plants showed similar phosphoproteins, which were different from those observed mcontrol.     

31P NMR of tissue phospholipids: a comparison of three tissue pre-treatment procedures

Extracted tissue phospholipid 31P NMR profiles, obtained from individual porcine lenses subjected to two preservation procedures (acetone desiccation and freeze-drying) and a perchloric acid-extraction procedure, were compared to those from freshly excised lens specimens. Each profile yielded quantitative data on 12 lens phospholipids: PC, LPC, PC plas, PE, LPE, PE plas, PS, SPH, PI, LPI, PG, and CL. A specimen group size of at least 9 lenses was required for secure statistical inter-group comparisons by the Scheffé procedure, due to specimen 31P NMR profile variability, interpreted as arising from specimen biological variability. The phospholipid profiles of lenses preserved by acetone desiccation were essentially identical to those from the freshly excised control lenses. Freeze-dried lens profiles differed significantly in four components, while profiles from perchloric acid-extracted lenses differed in six. It is concluded that specimen preservation by acetone disiccation is a useful method for preserving tissue phospholipids for subsequent 31P NMR profile analysis, while freeze-drying is not. Lipid extraction following a tissue acid extraction is also of little or no value in the determination of tissue phospholipid profiles.     

Strain energy density as a rupture criterion for the kidney: impact tests on porcine organs, finite element simulation, and a baseline comparison between human and porcine tissues

High-velocity (up to 25 m/s) impact tests were performed on pig kidneys to characterize failure behavior at deformation rates associated with traumatic injury. Cylindrical tissue samples (n = 45) and whole perfused organs (n = 34) were impacted using both falling weights and a high-velocity pneumatic projectile impactor. Impact energy was incrementally increased until visible rupture occurred. The strain energy density failure threshold fell between 25 and 60 kJ/m3 for excised porcine tissue samples, and between 15 and 30 kJ/m3 for whole, perfused organs. The relationship between localized failure in whole organ impacts and tissue level failure thresholds observed in cylindrical tissue samples was explored using a detailed finite element model of the human kidney. The model showed good correlation between experimentally observed injury patterns and predicted strain energy density distributions within the renal parenchyma. Finally, to facilitate interpretation of the porcine renal impact results with regard to human trauma, quasi-static compression test results of freshly excised human kidney cortex samples (n = 30) were compared against similar tests on pig kidneys. Human tissues failed at Lagrange strain levels similar to porcine tissue (63+/-6.3%), but at 52% lower Lagrange stress (116+/-28 kPa), and 35% lower strain energy density (17.1+/-4.4 kJ/m3). Thus conservative interpretation of porcine test results is recommended.     

Endogenous ethylene production is a potential problem in the measurement of nitrogenase activity associated with excised corn and sorghum roots

Endogenous ethylene production was evaluated as a source of ethylene during acetylene reduction assays with freshly collected roots of field-grown corn, Zea mays L. cv Funks G-4646, and sorghum, Sorghum bicolor (L.) Moench. cv CK-60A. Ethylene production was not detected when roots were incubated in air without acetylene. The presence of endogenous ethylene production was confirmed when roots were incubated anaerobically and in the presence of 40 millimolar sodium hydrosulfite. Ethylene oxidase activity was also associated with excised roots. The rate of ethylene oxidation was higher than the rates of ethylene accumulation during either acetylene reduction assays or anaerobic incubations. These results indicate that the procedure of incubating roots of grasses in air to monitor endogenous ethylene production is not a valid control in acetylene reduction studies with grasses. The presence of endogenous ethylene production during acetylene reduction assays was demonstrated by using either CO to inhibit nitrogenase activity or chloramphenicol to inhibit nitrogenase synthesis in freshly excised roots.     

Fast-green staining of interphase nucleoli in lemon fruit explants

Summary

Interphase nucleoli of freshly excised lemon fruit tissue showed a weak staining reaction with alkaline fast-green compared with that of enlarged interphase nucleoli of 48-hour-old tissue explants. Fast-green staining bodies were seen at various regions along the chromatin strands of the interphase nuclei of freshly excised tissue but absent from those of the 48-hour-old explants where nucleolar enlargement had occurred. The changes following tissue explanation are considered to indicate activation of the genome in response to the new environment.     

Frequency dispersions of human skin dielectrics.

The electrical properties of many biological materials are known to exhibit frequency dispersions. In the human skin, the impedance measured at various frequencies closely describes a circular locus of the Cole-Cole type in the complex impedance plane. In this report, the formative mechanisms responsible for the anomalous circular-arc behavior of skin impedance were investigated, using data from impedance measurements taken after successive strippings of the skin. The data were analyzed with respect to changes in the parameters of the equivalent Cole-Cole model after each stripping. For an exponential resistivity profile (Tregear, 1966, Physical Functions of Skin; Yamamoto and Yamamoto, 1976, Med. Biol. Eng., 14:151--158), the profile of the dielectric constant was shown to be uniform across the epidermis. Based on these results, a structural model has been formulated in terms of the relaxation theory of Maxwell and Wagner for inhomogeneous dielectric materials. The impedance locus obtained from the model approximates a circular are with phase constant alpha = 0.82, which compares favorably with experimental data. At higher frequencies a constant-phase, frequency-dependent component having the same phase constant alpha is also demonstrated. It is suggested that an approximately rectangular distribution of the relaxation time over the epidermal dielectric sheath is adequate to account for the anomalous frequency characteristics of human skin impedance.     

Beta-adrenergic receptors and stimulatory effects of (-) isoproterenol on testosterone production in fetal mouse Leydig cells

Beta-adrenergic receptors were characterized in freshly excised fetal mouse testis using the radioiodinated antagonist iodocyanopindolol (ICYP). [125I]-CYP bound to a single class of high affinity sites with a KD value of 42.2 +/- 7.0 pM. Adrenergic agonists competed for ICYP binding sites with the following order of potency: (-)isoproterenol greater than (-)epinephrine much greater than (-)norepinephrine which is typical for a beta 2-adrenergic receptor. A selective beta 2-receptor antagonist ICI 118-551 showed an approximately 200 fold higher affinity than the beta 1-selective compound, betaxolol. The beta-adrenergic agonist (-)isoproterenol did not or slightly affect testosterone production by freshly isolated fetal Leydig cells. The ability of fetal Leydig cells to respond to (-)isoproterenol increased during culture. This change in responsiveness was not accompanied either by modification of the number of binding sites or by change in the binding affinity. Taken together these data suggest that i) the stimulatory effect of (-)isoproterenol on testosterone production by cultured fetal Leydig cells is mediated through beta 2-adrenergic receptors ii), the inability of freshly Leydig cells to respond to catecholamines is probably due to post receptor events.     

Quantitative Analysis of Microbicide Concentrations in Fluids,Gels and Tissues Using Confocal Raman Spectroscopy

Topical vaginal anti-HIV microbicides are an important focus in female-based strategies to prevent the sexual transmission of HIV. Understanding microbicide pharmacokinetics is essential to development, characterization and implementation of efficacious microbicide drug delivery formulations. Current methods to measure drug concentrations in tissue (e.g., LC-MS/MS, liquid chromatography coupled with tandem mass spectrometry) are highly sensitive, but destructive and complex. This project explored the use of confocal Raman spectroscopy to detect microbicide drugs and to measure their local concentrations in fluids, drug delivery gels, and tissues. We evaluated three candidate microbicide drugs: tenofovir, Dapivirine and IQP-0528. Measurements were performed in freshly excised porcine buccal tissue specimens, gel vehicles and fluids using two Horiba Raman microscopes, one of which is confocal. Characteristic spectral peak calibrations for each drug were obtained using serial dilutions in the three matrices. These specific Raman bands demonstrated strong linear concentration dependences in the matrices and were characterized with respect to their unique vibrational signatures. At least one specific Raman feature was identified for each drug as a marker band for detection in tissue. Sensitivity of detection was evaluated in the three matrices. A specific peak was also identified for tenofovir diphosphate, the anti-HIV bioactive product of tenofovir after phosphorylation in host cells. Z-scans of drug concentrations vs. depth in excised tissue specimens, incubated under layers of tenofovir solution in a Transwell assay, showed decreasing concentration with depth from the surface into the tissue. Time-dependent concentration profiles were obtained from tissue samples incubated in the Transwell assay, for times ranging 30 minutes - 6 hours. Calibrations and measurements from tissue permeation studies for tenofovir showed good correlation with gold standard LC-MS/MS data. These results demonstrate that confocal Raman spectroscopy holds promise as a tool for practical, minimally invasive, label-free measurement of microbicide drug concentrations in fluids, gels and tissues.     

Multiphoton Multispectral Fluorescence Lifetime Tomography for the Evaluation of Basal Cell Carcinomas

We present the first detailed study using multispectral multiphoton fluorescence lifetime imaging to differentiate basal cell carcinoma cells (BCCs) from normal keratinocytes. Images were acquired from 19 freshly excised BCCs and 27 samples of normal skin (in & ex vivo). Features from fluorescence lifetime images were used to discriminate BCCs with a sensitivity/specificity of 79%/93% respectively. A mosaic of BCC fluorescence lifetime images covering >1 mm² is also presented, demonstrating the potential for tumour margin delineation. Using 10,462 manually segmented cells from the image data, we quantify the cellular morphology and spectroscopic differences between BCCs and normal skin for the first time. Statistically significant increases were found in the fluorescence lifetimes of cells from BCCs in all spectral channels, ranging from 19.9% (425–515 nm spectral emission) to 39.8% (620–655 nm emission). A discriminant analysis based diagnostic algorithm allowed the fraction of cells classified as malignant to be calculated for each patient. This yielded a receiver operator characteristic area under the curve for the detection of BCC of 0.83. We have used both morphological and spectroscopic parameters to discriminate BCC from normal skin, and provide a comprehensive base for how this technique could be used for BCC assessment in clinical practice.     

Effect of cryostorage on oxygen uptake and autograft viability of rat skin

The pre- and post-thawing oxygen uptake of rat skin treated with either 0.9% NaCl or 10% DMSO was compared with the gross survival of skin autografts. Little change was observed in the average oxygen consumption of freshly excised samples taken 28 days apart. Soaking for 2 hr in 10% DMSO decreased oxygen consumption about 29% and freeze-thawing caused a further decrease in oxygen uptake. DMSO soaked, frozen and thawed grafts (studied 28 days after grafting) had a 12% higher oxygen utilization than freshly excised skin. Only 5 of 19 autografts soaked in 0.9% NaCl became functional, but 21 of 38 skin samples soaked in 10% DMSO became functional autografts. The oxygen consumption of the 21 takes was not significantly different from the non-takes. An analysis of variance showed that oxygen utilization of skin subsamples could not reliably predict autograft viability after freeze-storage.     

Isolation and cell-free translation of chick lens crystallin mRNA during normal development and transdifferentiation of neural retina

Messenger RNA has been isolated from day-old chick lens. Size characterization and heterologous cell-free translation demonstrate that the predominant species of mRNA present code for α-, β- and δ-crystallins. Total polysomal RNA and polysomal RNA which did not bind to oligo (dT)-cellulose translate in the cell-free system to give a crystallin profile qualitatively similar to that of poly(A)⁺ mRNA. RNA from postribosomal supernatant which binds to oligo(dT)-cellulose also translates to give crystallins, but the products are enriched for β-crystallins. Messenger RNAs isolated from 15-day embryo lens fiber and lens epithelium cells give products on translation which reflect the different protein compositions of these two cell types, as do mRNAs isolated from chick lenses at various developmental stages. Messenger RNAs were isolated from freshly excised 8-day embryo neural retina and from this tissue undergoing transdifferentiation into lens cells in cell culture. Cell-free translation demonstrates no detectable crystallin mRNAs in the freshly excised material, but by 42 days in cell culture, crystallin mRNAs are the most prominent species.     

离体蒜苔衰老过程中乙烯产生和纤维素酶活力的变化

自Horton和Osborne(1967)报道衰老、脱落中激素和纤维素酶活力相关性以来,许多实验证明,乙烯和纤维素酶与衰老和脱落有密切关系。关颖谦等(1981)指明离体水稻叶片衰老时,纤维素酶的活力     

Effect of the hypocotyl hook on greening in etiolated cucumber cotyledons

Four-day-old etiolated cucumber cotyledons (Cucumis sativus, L.) were excised and allowed to green in white fluorescent light at 28 C. Cotyledons excised with a full hypocotyl hook exhibited a lag phase of 1 hour before entering the rapid greening phase, whereas cotyledons excised without any hypocotyl hook exhibited a lag phase of 6 hours. Cotyledons excised with varying lengths of hypocotyl hook accumulated chlorophyll roughly in proportion to the hook length. When cotyledons were excised with a full hook and were partially or totally shielded from light with aluminum foil, the samples with the hook covered accumulated more chlorophyll than the wholly exposed samples. The samples with the cotyledons covered showed no net accumulation of chlorophyll irrespective of hook's exposure to light. These data suggest the contribution of some factor or factors by the hypocotyl hook which reduce the lag phase during greening.     

Aged preparations are electrophysiologically more representative of intact tissue than are freshly excised preparations

Studies using excised tissues usually suffer from a discrepancy in the results between freshly excised preparations and aged ones (i.e. preparations which are allowed to rest and-or regenerate for about a day between excision and experimentation). This is especially true for measurements of the membrane potential (V_m) and its changes upon exposure to light in slices of extensor tissue of the laminar pulvini of Phaseolus coccineus L. Measurements of the V _m of extensor cells in situ reveal virtually identifical results to those obtained from aged excised preparations (more negative resting V _m; dramatic, light-induced transients of V _m), whereas freshly excised preparations display a small and light-insensitive V _m. It is concluded, therefore, that for the given example aged preparations are more suitable than fresh ones for investigating the properties of intact tissues.Symbol V_m membrane potential     

An experimental study of the dielectric dispersion of solutions of cytochrome c at medium ionic strengths

In this paper, the results are presented of measurements of the dielectric dispersions of horse heart cytochrome c molecules in various buffers. The data are fitted to the Cole-Cole relaxation model. The influence of the concentration and the ionic strength on the parameters that result from the Cole-Cole model is determined. The measured data are compared with calculations based on the model presented previously. Good agreement is found between the model and the observed data.     

Pollen analysis as a means to determine the geographical origin of royal jelly

In this study we investigated the use of pollen analysis as a method to determine the geographical origin of royal jelly. We recorded the pollen flora sampled by bees using pollen traps for two consecutive years and we also collected and examined royal jelly samples from the same apiary. For royal jelly production, bees mainly used the freshly collected pollen. All major pollen types that were recorded in the area using pollen traps were also detected in the royal jelly samples. Thus, pollen analysis can be used as a method to determine the geographical origin of royal jelly.     

An Analysis of the Relationship between Respiration and the Transmembrane Potential in Corn Roots

The effects of cyanide, anoxia, and temperatures varying from 2 to 42 C on the cell membrane electropotential difference (PD) of washed and freshly excised corn roots have been determined. Respiration rates of freshly excised root segments in response to cyanide and to varying temperatures were also measured. The cell membrane PD of roots which had been washed for 12 to 15 hours was almost insensitive to cyanide and anoxia but sensitive to low temperature. In contrast, the cell membrane PD of freshly excised roots was reversibly depolarized by all three treatments, cyanide depolarized from −117 to −86 millivolts and the sequential imposition of anoxia further lowered the PD to −69 millivolts. Anoxia applied first depolarized maximally and the PD was not further lowered by sequential cyanide treatment. Arrhenius plot analysis of the temperature response of respiration showed an apparent transition at 13 C with an activation energy of 20.0 kilocalories per mole below and 8.8 kilocalories per mole above the transition temperatures. The energy of activation for repolarization of PD is much higher; 53.4 kilocalories per mole below 7 to 8 C and 25.4 kilocalories per mole above this apparent transition. The energy requirement for polarization of the cell membrane PD was calculated based on the temperature responses of the cell membrane PD and respiration. It was estimated that 3.5% of the energy output from respiration at 22 C is required for cell polarization. It is unlikely that ion transport is limited by energy availability below the 8 C transition in this chill sensitive species.     

RNA在离体小鼠肝脏组织中的稳定性

采取肝脏等临床样本时,常因不能及时保存造成核酸降解,从而影响后续实验的进行.本研究旨在通过对室温条件下放置不同时间的小鼠肝脏组织的RNA的完整性进行评价,为肝脏临床样本的采集与保存提供依据.将离体小鼠肝脏组织在室温下放置0～180min后,提取总RNA,采用电泳、RT-PCR和芯片生物分析仪检测RNA的完整性.电泳结果显示,将小鼠肝脏置于室温180min后,RNA尚未发生降解.对β肌动蛋白,GAPDH和Trp53的RT-PCR的分析表明,室温下保存180min的RNA样品均未降解.生物分析仪检测的RNA完整性系数(RIN)都大于7.9,样品可用于后续研究.因此,离体后的小鼠肝脏置于室温下3h以内,RNA仍能保持其完整性.     

Variability in Juvenile Hormone production by locust corpora allata kept in vitro for long periods

Abstract. Juvenile Hormone III (JH-III) production by corpora allata (CA) of sexually mature female locusts (Locusta migratoria migratorioides (R. & F.)) was maintained in vitro for up to 30 days in an agar-solidified medium. Hormone production was measured periodically with a short-term radiochemical assay. Low-activity CA increased their activity significantly after 24–48 h incubation in the long-term medium, but high-activity glands did not. Variations in activity were considerable among glands tested on the same day and among measurements from the same gland on different days. Farnesoic acid-stimulated rates of JH-III production were always higher than the basal rates, suggesting that the CA were not maximally activated. However, freshly excised low-activity CA, whose hormone production increased in the long-term conditions, showed similar farnesoic acid-stimulated rates of JH-III production to those of freshly excised high-activity glands, suggesting that at the time of excision of the corpora allata rate-limiting step(s) preceding farnesoic acid biosynthesis were inhibited or refractory to stimulation in vivo.