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大鼠肝细胞中糖原和磷酸化酶活性的电子显微镜显示

Electron microscopic demonstration of glycogen and phosphorylase activity in rat hepatocytes.

作者信息

Lindberg L A, Palkama A

出版信息

Histochem J. 1977 May;9(3):277-84. doi: 10.1007/BF01004763.

DOI:10.1007/BF01004763
PMID:863745
Abstract

The effect of fixation with a bicarbonate-buffered solution of paraformaldehyde and polyvinyl pyrrolidone (PVP) on the ultrastructural demonstration of glycogen and phosphorylase activity in rat hepatocytes has been studied. Phosphorylase was demonstrated by the precipitation of liberated phosphate ions with ferrous ions. 7.5% PVP was included in all steps in the procedure before post-fixaiton in osmium tetroxide. Glycogen particles were well preserved. Structures connecting membranes and glycogen particles were also evident. Phosphorylase activity was rapidly inhibited by the fixative; the fixation time was, therefore, kept very short. The final reaction product was localized on glycogen particles and on endoplasmic membranes in association with glycogen particles. The results support the view that endoplasmic membranes are involved in the metabolism of glycogen in hepatocytes.

摘要

研究了用多聚甲醛和聚乙烯吡咯烷酮(PVP)的碳酸氢盐缓冲溶液固定对大鼠肝细胞糖原和磷酸化酶活性超微结构显示的影响。通过亚铁离子沉淀游离磷酸根离子来显示磷酸化酶。在四氧化锇后固定之前的所有步骤中都加入7.5%的PVP。糖原颗粒保存良好。连接膜和糖原颗粒的结构也很明显。固定剂能迅速抑制磷酸化酶活性;因此,固定时间保持非常短。最终反应产物定位于糖原颗粒以及与糖原颗粒相关的内质膜上。这些结果支持内质膜参与肝细胞糖原代谢的观点。

相似文献

1
Electron microscopic demonstration of glycogen and phosphorylase activity in rat hepatocytes.大鼠肝细胞中糖原和磷酸化酶活性的电子显微镜显示
Histochem J. 1977 May;9(3):277-84. doi: 10.1007/BF01004763.
2
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Histochem J. 1995 Aug;27(8):609-14.
4
The 'chess board' distribution of glycogen in liver. Artifact of fixation or the effect of an enzyme?
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J Cell Biol. 1979 Nov;83(2 Pt 1):348-56. doi: 10.1083/jcb.83.2.348.
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Electron microscopic demonstration of rat liver glycogen phosphorylase activity with iron (Fe++).用铁(Fe++)对大鼠肝脏糖原磷酸化酶活性进行电子显微镜演示。
Histochemistry. 1974 Mar 13;38(4):285-96. doi: 10.1007/BF00496717.
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Histochemical demonstration of rat liver glycogen phosphorylase activity with iron (Fe++).用铁(Fe++)对大鼠肝脏糖原磷酸化酶活性进行组织化学显示。
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本文引用的文献

1
Preservation of the fine structure of isolated liver cell particulates with polyvinylpyrrollidone-sucrose.用聚乙烯吡咯烷酮-蔗糖保存分离的肝细胞微粒体的精细结构。
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[Formation of endoplasmic membranes in liver parenchymal cells in vitro. IV. Demonstration of membrane building stones in "glycogen complexes" of the liver parenchymal cell].[体外肝实质细胞内质膜的形成。IV. 肝实质细胞“糖原复合物”中膜构建结石的证实]
Acta Biol Med Ger. 1969;23(6):887-906.
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Role of the sarcoplasmic reticulum in glycogen metabolism. Binding of phosphorylase, phosphorylase kinase, and primer complexes to the sarcovesicles of rabbit skeletal muscle.
肌浆网在糖原代谢中的作用。磷酸化酶、磷酸化酶激酶和引物复合物与兔骨骼肌肌浆囊泡的结合。
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Effects on tissue fine structure of variations in colloid osmotic pressure of glutaraldehyde fixatives.
J Ultrastruct Res. 1970 Jan;30(1):195-208. doi: 10.1016/s0022-5320(70)90073-0.
5
Histochemical demonstration of rat liver glycogen phosphorylase activity with iron (Fe++).用铁(Fe++)对大鼠肝脏糖原磷酸化酶活性进行组织化学显示。
Histochemie. 1973;36(4):355-65. doi: 10.1007/BF00305714.
6
Lead and some other metals in the histochemical demonstration of rat liver glycogen phosphorylase activity.
Histochemie. 1973;36(4):347-53. doi: 10.1007/BF00305713.
7
Electron microscopy and phosphorylase reactions.电子显微镜检查与磷酸化酶反应
Ann N Y Acad Sci. 1973 Feb 9;210:46-50. doi: 10.1111/j.1749-6632.1973.tb47560.x.
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An enzymic method for measurement of glycogen.一种测定糖原的酶法。
Anal Biochem. 1967 May;19(2):315-26. doi: 10.1016/0003-2697(67)90167-4.
9
Electron microscopic demonstration of rat liver glycogen phosphorylase activity with iron (Fe++).用铁(Fe++)对大鼠肝脏糖原磷酸化酶活性进行电子显微镜演示。
Histochemistry. 1974 Mar 13;38(4):285-96. doi: 10.1007/BF00496717.
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Effect of pH in direct OsO 4 fixation on glycogen staining as shown by electron microscopy.
Stain Technol. 1972 Jan;47(1):39-40. doi: 10.3109/10520297209116534.