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31.
A. Shteyer D. Gazit I. Binderman I. A. Bab 《In vitro cellular & developmental biology. Plant》1987,23(1):15-20
Summary Cells of the dental papilla are capable of odontoblastic, fibroblastic, and endothelial differentiation and formation of dentin
and the dental pulp. In the present study dental papilla cells, obtained from human tooth buds (HDP cells), were cultured
in vitro through 3 to 7 passages. After exposure to prostaglandin E2 there was a marked decrease in intracellular cyclic AMP (cAMP) levels as compared to hormone-free controls. Parathyroid hormone
and calcitonin had stimulatory effects with 1 and 2 log increases in cAMP, respectively. The HDP cells showed moderate activity
of alkaline phosphatase, 1 log higher than that of hamster kidney fibroblasts (BHK 13) and 1 log lower than that of osteoblastic
osteosarcoma cells (ROS 17/2). When cultured for 4 or 8 wk in diffusion chambers (DC) implanted in athymic mice, many of the
HDP cells underwent odontoblastic morphodifferentiation with very long, single processes extending into the matrix. This matrix
contained banded and unbanded collagen fibers. Neither light nor electron microscopy of the DC content revealed mineral deposits.
These results suggest that HDP cells have an intrinsic potential for partial odontoblastic differentiation; inductive signals
like those originating from odontogenic epithelium are probably essential for the completion of hard tissue formation. 相似文献
32.
Dephosphorylation and reactivation of phosphorylated purified ox-kidney branched-chain dehydrogenase complex by co-purified phosphatase 总被引:7,自引:0,他引:7
The branched-chain 2 oxoacid dehydrogenase complex has been purified from well-washed ox-kidney mitochondria together with branched-chain dehydrogenase kinase. The complex was inactivated and phosphorylated by ATP in about 5 min at 30 degrees C. After hydrolysis of ATP by a contaminating ATPase (5-10 min) the complex was dephosphorylated and reactivated. Dephosphorylation and reactivation were linearly correlated. Reactivation was dependent upon Mg2+ (K0.5 greater than 1 mM) and inhibited completely by 50 mM fluoride. Reactivation and dephosphorylation are attributed to a mitochondrial branched-chain dehydrogenase phosphatase. 相似文献
33.
Metabolic acidosis produces a phosphaturia which is independent of parathyroid hormone or dietary phosphorus intake. To study the underlying mechanism, inorganic phosphate (Pi) and glucose transport were studied in brush-border membrane vesicles prepared from the renal cortex of parathyroidectomized rats gavaged for three days with either 7.5 ml of 1.6% NaCl (control) or 1.5% NH4Cl (acidosis). At killing, blood pH and plasma bicarbonate were and , respectively, in control and () and () in acidotic rats. Serum Pi was similar in both groups, while 24 h urine Pi excretion was higher in the acidotic group (). Peak sodium-dependent uptake of Pi, measured after 1.5 min of incubation, was higher in controls than acidotic rats ( vs. protein, ), whereas peak glucose uptake at 1.5 min was not significantly different between the groups. Equilibrium values for Pi and glucose uptake were similar in the two groups. for Pi uptake in the control and acidotic animals were not different, 0.036 and 0.040 mM, respectively. By contrast, was higher in controls than in the acidotic group, 3.13 vs. 1.15 nmol/mg protein per 15 s. These results suggest that metabolic acidosis directly inhibits Pi uptake by the brush border of the proximal tubule by decreasing the availability of Pi carriers of the renal brush-border membrane. 相似文献
34.
Acid phosphatase purified from maize scutellum, upon acylation with succinic anhydride, still shows negative co-operativity for the hydrolysis of glucose-6-phosphate at pH 5.4. This phenomenon is abolished by glucose, for both native and succinylated enzymes, through stimulation of the initial velocities at sub-optimal substrate concentrations. However, negative co-operativity for the enzymatic hydrolysis of p-nitrophenylphosphate at pH 5.4 is suppressed only at high concentrations of glucose. Furthermore, the hydrolysis of p-nitrophenylphosphate is noncompetitively inhibited (low affinity form of the enzyme molecule) by glucose, which suggests the existence of different substrate binding sites. 相似文献
35.
Jean J. Pasteels 《Cell and tissue research》1969,102(4):594-600
Résumé Dans toutes les cellules mucipares de la branchie de Mytilus edulis L., quelques grains de secretion montrent une activité phosphatasique acide, décelée par la méthode cytochimique de Gomori appliquée au microscope électronique. A la proximité de ces grains se trouvent des dictyosomes golgiens où une activité phosphatasique se décèle dans les parties latérales des cisternes et dans les vésicules qui en émanent. Au moment de l'excrétion, tous les grains de sécrétion confluent et la phosphatase acide active est incluse dans l'amas de mucus expulsé dans la cavité palléale. Le rôle digestif de ces amas — et non purement mécanique — peut ainsi être considéré comme hautement probable. De telles manifestations enzymatiques sont totalement absentes dans le tapis muqueux ainsi que dans les cellules qui le constituent.
Excretion of acidic phosphatase by the goblet-cells of the gill of Mytilus edulis L.An electron microscopic study
Summary Acidic phosphatase activity detected by the Gomori method applied to E.M., has been found in a few secretion granules of each goblet cell of the gill of Mytilus edulis L. In the close proximity of those granules golgian dictyosomes always occur, with acidic phosphatase activity in the lateral parts of the cisternae and in the vesicles arising from the latter. When the mucus is extruded, active and non active secretion granules are mixed and thus, acidic phosphatase activity is regularly found in the mucous tufts extruded into the palleal cavity. Therefore the digestive role — and not merely mechanic — of the mucous tufts may be considered as highly probable. Conversely, the secretion granules from which arises the continuous mucous cover of the epithelium and this cover also, are entirely devoid of any acidic phosphatase activity.相似文献
36.
Ruth Schwaninger Eric Dumermuth M. Ernst Schweingruber 《Molecular & general genetics : MGG》1990,221(3):403-410
Summary Structural gene mutants of the cell-surface glycoprotein acid phosphatase of Schizosaccharomyces pombe were analysed to define structural determinants that are responsible for enzymatic activity, N-glycosylation and secretion. All seven defined mutations cause a single amino acid substitution in the mature acid phosphatase protein and destroy the enzymatic activity. The mutational lesions are distributed throughout the pho1 gene. A ser to phe substitution at position 349 abolishes enzymatic activity only and does not affect glycosylation and secretion. Two mutations create a new N-glycosylation site by substitution of pro at position 56 by phe and ser, respectively. This new site is apparently used in the mutants. Their core-glycosylated acid phosphatase is slightly larger than that of the wild type. Overglycosylation seems not to affect secretion. Four different mutations (a gly to asp substitution at position 281 and ser to phe substitutions at positions 150, 271 and 277) cause intracellular accumulation of enzymatically inactive core-glycosylated acid phosphatase precursor. These mutational lesions apparently block transport of acid phosphatase from the endoplasmic reticulum to the Golgi apparatus. 相似文献
37.
Hae-Jin Chung Christopher Shaffer Ross MacIntyre 《Molecular & general genetics : MGG》1996,250(5):635-646
InDrosophila, unlike humans, the lysosomal acid phosphatase (Acph-1) is a non-essential enzyme. It is also one of the most rapidly evolving gene-enzyme systems in the genus. In order to determine which parts of the enzyme are conserved and which parts are apparently under little functional constraint, we cloned the gene fromDrosophila melanogaster via a chromosomal walk. Fragments from the gene were used to recover an apparently full-length cDNA. The cDNA was subcloned into aDrosophila transformation vector where it was under the control of the 5 promoter sequence of thehsp-70 gene. Three independent transformants were obtained; in each, Acph-1 expression from the cDNA was constitutive and not dependent on heat shock, as determined by densitometric analyses of the allozymic forms of the enzyme. The pattern of expression indicates thehsp-70 and endogenousAcph-1 promoters act together in some, but not all, tissues. The sequence of the cDNA was determined using deletions made with exonuclease III, and primers deduced from the cDNA sequence were used to sequence the genomic clone. Five introns were found, and putative 5 up-stream regulatory sequences were identified. Amino acid sequence comparisons have revealed several highly conserved motifs betweenDrosophila Acph-1 and vertebrate lysosomal and prostatic acid phosphatases. 相似文献
38.
Takako S. Kaneko Mamiko Sato Masako Osumi Makoto Muroi Akira Takatsuki 《Plant cell reports》1996,15(6):409-413
Summary The effects of brefeldin A (BFA) on the secretion of acid phosphatase (APase) by tobacco protoplasts were investigated. Secretion of APase was inhibited by BFA in a dose-dependent manner, with a concomitant intracellular accumulation of the enzyme. The secreted APase was composed of two isoforms. BFA (10/ g/ml) inhibited the secretion of one of the isoforms without inhibiting that of the other, and this phenomenon explains the partial inhibition of APase secretion as a whole. The inhibition of APase secretion was accompanied by changes in the morphology of the Golgi apparatus and also by an increment in massdensity of cells.Abbreviations APase
acid phosphatase
- BFA
brefeldin A
- CHX
cycloheximide
- PAGE
polyacrylamide gel electrophoresis 相似文献
39.
大豆子叶内酸性磷酸酶活性的超微结构定位 总被引:6,自引:0,他引:6
开花后35~50 d 期间和萌发早期(播种后4~8 d)的大豆(Glycinem ax L.)种子中,酸性磷酸酶主要分布在子叶细胞中的蛋白体内;在内质网内也检测到酸性磷酸酶活性。此外,在萌发早期的部分子叶细胞的质膜外侧及其细胞壁基质中可见密集的酸性磷酸酶活性;而且在近质膜的胞质中常见到一些富含磷酸铅沉淀的胞质小泡,似与质膜融合 相似文献
40.
遗传标记与数量性状基因间连锁关系的分析 总被引:2,自引:0,他引:2
本文讨论标记基因与数量性状主基因连锁关系的一般分析方法,包括重组值的估计和有关遗传假设的测验。并以我们水稻遗传试验中两个具有互补和重叠作用的卷叶基因和一个矮秆基因试验结果的分析为例作了较详细的示范。 相似文献