Safer A M, Abou-Salem K
Department of Zoology, Faculty of Science, University of Kuwait, Kuwait.
Anat Histol Embryol. 1997 Mar;26(1):29-34. doi: 10.1111/j.1439-0264.1997.tb00099.x.
Phosphatase cytochemical activity in the normal glomerulus of the desert gerbil Meriones crassus was demonstrated using cerium ions as capturing agents. Three major enzymes have been recognized: sodium-potassium adenosine triphosphatase (Na(+)-K(+)-ATPase), alkaline phosphatase (ALPase) and acid phosphatase (ACPase). However, cytochemical staining for these markers to map their localizations and distributions reveal a high positivity of Na(+)-K(+)-ATPase. This appeared as uniform dense precipitates surrounding the glomerular basement membrane (GBM) and the plasma membranes of the epithelial and endothelial cells of the glomerular layers. Negligible ALKase reaction product being over the glomerular epithelia including the GBM. In contrast, the cytochemical profiles of ACPase was unusual, with dense reaction products extensively covering the endoplasmic reticulum at the region of Golgi apparatus products lysosomes (GERL) complex, including its cisternal and tubular elements and the lysosomal-vacuolar apparatus of the glomerular epithelial cells. All other subcellular organelles showed no activity. For Na(+)-K(+)-ATPase, the reaction product was successive when acetate buffer (as decalcifying agent, pH 5.0) was used. This reaction was still seen when a medium containing levamisole was used. Cytochemical controls for all enzymes were incubated in substrate-free media including those using levamisole as an inhibitor of ALPase. The data presented, which is reported for the first time, is not an attempt to determine the contribution of the selected phosphatases in the glomerular physiology and pathology. Such findings may, nevertheless, have functional implications in the fact that these markers may be involved in the ultrafiltration and other metabolic activities of the glomerulus at the molecular and/or cellular level. In addition to earlier morphological and recent histochemical work, the present study updates and recognizes information to be used as a baseline to which the gerbil model can now be employed to investigate the behavioural adaptations of the desert rodents.
使用铈离子作为捕获剂,证明了厚尾沙鼠正常肾小球中的磷酸酶细胞化学活性。已识别出三种主要酶:钠钾三磷酸腺苷酶(Na(+)-K(+)-ATPase)、碱性磷酸酶(ALPase)和酸性磷酸酶(ACPase)。然而,对这些标志物进行细胞化学染色以绘制其定位和分布,结果显示Na(+)-K(+)-ATPase呈高度阳性。这表现为围绕肾小球基底膜(GBM)以及肾小球层上皮细胞和内皮细胞质膜的均匀致密沉淀物。在包括GBM在内的肾小球上皮细胞上,碱性磷酸酶反应产物可忽略不计。相比之下,酸性磷酸酶的细胞化学图谱不同寻常,致密的反应产物广泛覆盖了高尔基体产物溶酶体(GERL)复合体区域的内质网,包括其扁平囊和管状成分以及肾小球上皮细胞的溶酶体-液泡装置。所有其他亚细胞器均无活性。对于Na(+)-K(+)-ATPase,使用乙酸盐缓冲液(作为脱钙剂,pH 5.0)时反应产物是连续的。使用含有左旋咪唑的培养基时仍可看到这种反应。所有酶的细胞化学对照均在无底物的培养基中孵育,包括使用左旋咪唑作为碱性磷酸酶抑制剂的培养基。首次报道的这些数据并非试图确定所选磷酸酶在肾小球生理和病理中的作用。然而,这些发现可能具有功能意义,因为这些标志物可能在分子和/或细胞水平上参与肾小球的超滤和其他代谢活动。除了早期的形态学和近期的组织化学研究外,本研究更新并确认了相关信息,可作为现在使用沙鼠模型研究沙漠啮齿动物行为适应性的基线。