The fine structural localization of testicular phosphatases in man: The control testis
- 1 February 1976
- journal article
- research article
- Published by Springer Nature in Cell and tissue research
- Vol. 166 (4) , 497-510
- https://doi.org/10.1007/bf00225914
Abstract
Summary Electron microscopic cytochemistry was used to determine the localization of five phosphatase enzymes—glucose-6-phosphatase, inosine diphosphatase, thiamine pyrophosphatase, acid phosphatase, and adenosine triphosphatase—in control human testes. Glucose-6-phosphatase occurred in the endoplasmic reticulum and nuclear envelope of Sertoli cells, Leydig cells and primitive spermatogonia, but was not observed in more advanced spermatogenic cells. The presence of glucose-6-phosphatase activity paralleled the presence of glycogen in spermatogenic cells, i.e., both occurred in type AL and AD spermatogonia but not in type AP or B spermatogonia or in more advanced spermatogenic cells. Inosine diphosphatase activity was found in the endoplasmic reticulum, nuclear envelope, and Golgi complex of Sertoli cells and all spermatogenic cells except late spermatids. Additionally, inosine diphosphatase activity was localized at the junctions between Sertoli cells and late spermatids, but was not associated with any other plasma membrane. Thiamine pyrophosphatase reaction product was found in the Golgi bodies of Sertoli cells and in spermatogenic cells through immature spermatids. Neither inosine diphosphatase nor thiamine pyrophosphatase was observed in the Golgi bodies of spermatids during acrosomal formation. Acid phosphatase activity was found in lysosomes of spermatogonia, spermatocytes, and spermatids, in lysosomes of Leydig cells, and in lysosomes, lipofuscin bodies, and Golgi cisternae of Sertoli cells. It is thought that Sertoli lysosomes play a role in the phagocytosis of degenerating germ cells; however, the role of spermatogenic or Leydig lysosomes is unknown. Adenosine triphosphatase activity occurred at the interfaces between two spermatogonia, and between Sertoli cells and spermatogonia, but was not observed in the spaces between two Sertoli cells, two spermatocytes, two spermatids, or between Sertoli cells and spermatocytes, or between Sertoli cells and spermatids.Keywords
This publication has 29 references indexed in Scilit:
- A low-viscosity epoxy resin embedding medium for electron microscopyPublished by Elsevier ,2004
- Electron Microscopic Cytochemical Study of Phosphatases During Spermiogenesis in Chinese Hamster1Biology of Reproduction, 1974
- Organization and Redistribution of Adenosinetriphosphatase During Spermiogenesis in the MouseBiology of Reproduction, 1974
- Localization of phosphatase activity on the membranes of the mammalian sperm headJournal of Experimental Zoology, 1973
- The fine structure of nuclei as revealed by electron microscopyExperimental Cell Research, 1967
- THE DEMONSTRATION OF ENZYMATIC ACTIVITY IN PINOCYTIC VESICLES OF BLOOD CAPILLARIES WITH THE ELECTRON MICROSCOPEThe Journal of cell biology, 1963
- THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- CYTOCHEMISTRY AND ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- IMPROVEMENTS IN EPOXY RESIN EMBEDDING METHODSThe Journal of cell biology, 1961
- Spermiogenesis of man, monkey, ram and other mammals as shown by the “periodic acid‐schiff” techniqueJournal of Anatomy, 1955