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大鼠肾皮质肾小管周细胞中促红细胞生成素mRNA与外切5'-核苷酸酶免疫反应性的共定位表明,成纤维细胞可产生促红细胞生成素。

Co-localization of erythropoietin mRNA and ecto-5'-nucleotidase immunoreactivity in peritubular cells of rat renal cortex indicates that fibroblasts produce erythropoietin.

作者信息

Bachmann S, Le Hir M, Eckardt K U

机构信息

Institut für Anatomie und Zellbiologie, Heidelberg, Germany.

出版信息

J Histochem Cytochem. 1993 Mar;41(3):335-41. doi: 10.1177/41.3.8429197.

Abstract

In adults, the kidneys are the major site of production of the glycoprotein hormone erythropoietin (EPO), but the type of renal cell producing EPO has not yet been identified. In the present study we used non-radioactive in situ hybridization with a digoxigenin-labeled cRNA probe to localize cells that produce erythropoietin (EPO) in kidneys of anemic rats. Cryostat sections from both native and perfusion-fixed tissue were used. Cells containing EPO mRNA were found exclusively in the peritubular space of the renal cortex. Using high-resolution interference contrast optics, we found that cells expressing EPO mRNA were not associated with the lumina of peritubular capillaries but rather were located in the angles between adjacent tubules or between tubules and vessels. These spaces are predominantly occupied by resident interstitial fibroblasts and by their cytoplasmic processes. To further identify the type of cell containing EPO mRNA, a double-labeling protocol was established that permitted on the same tissue section both in situ hybridization for EPO mRNA and parallel immunolabeling of ecto-5'-nucleotidase (5'-Nu), a surface marker of peritubular interstitial fibroblasts. The combined labeling technique revealed that a clear majority of cells expressing EPO mRNA also displayed staining for anti-5'-Nu. Staining for EPO mRNA was localized in central perinuclear parts of the interstitial cells, whereas 5'-Nu label was present on the cell surface, including the cytoplasmic processes. These data indicate that peritubular fibroblasts are cellular sites for production of erythropoietin.

摘要

在成年人中,肾脏是糖蛋白激素促红细胞生成素(EPO)的主要产生部位,但产生EPO的肾细胞类型尚未确定。在本研究中,我们使用地高辛配体标记的cRNA探针进行非放射性原位杂交,以定位贫血大鼠肾脏中产生促红细胞生成素(EPO)的细胞。使用了来自天然组织和灌注固定组织的低温恒温器切片。含EPO mRNA的细胞仅在肾皮质的肾小管周围间隙中发现。使用高分辨率干涉对比光学显微镜,我们发现表达EPO mRNA的细胞与肾小管周围毛细血管腔不相关,而是位于相邻肾小管之间或肾小管与血管之间的夹角处。这些间隙主要由常驻间质成纤维细胞及其细胞质突起占据。为了进一步确定含EPO mRNA的细胞类型,建立了一种双重标记方案,该方案允许在同一组织切片上同时进行EPO mRNA的原位杂交和肾小管周围间质成纤维细胞表面标志物ecto-5'-核苷酸酶(5'-Nu)的平行免疫标记。联合标记技术显示,表达EPO mRNA的细胞中绝大多数也显示出抗5'-Nu染色。EPO mRNA染色定位于间质细胞的核周中央部分,而5'-Nu标记存在于细胞表面,包括细胞质突起。这些数据表明肾小管周围成纤维细胞是促红细胞生成素的细胞产生部位。

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