Lacombe C, Da Silva J L, Bruneval P, Fournier J G, Wendling F, Casadevall N, Camilleri J P, Bariety J, Varet B, Tambourin P
Institut National de la Santé et de la Recherche Medicale (INSERM) U152, CNRS UA 628, Hôpital Cochin, Paris, France.
J Clin Invest. 1988 Feb;81(2):620-3. doi: 10.1172/JCI113363.
Erythropoietin (Epo)-producing cells were identified in the murine hypoxic kidney by in situ hybridization. Profound anemia was induced in order to greatly increase Epo production. This resulted in high levels of Epo mRNA in the kidney. 35S-labeled DNA fragments of the murine Epo gene were used as probes for in situ hybridization. Control experiments conducted in parallel included kidneys of nonanemic mice, RNase-treated hypoxic kidney sections, and 35S-labeled non-Epo-related DNA. The Epo probe gave a specific hybridization signal in the hypoxic kidney in the cortex and to a lesser extent in the outer medulla. Glomerular and tubular cells were not labeled. All positive cells were identified as peritubular cells. Using immunofluorescence, we showed that cells with the same topography contained Factor VIII-related antigen. These data demonstrated that peritubular cells, most likely endothelial cells, constitute the major site of Epo production in the murine hypoxic kidney.
通过原位杂交在小鼠缺氧肾脏中鉴定出促红细胞生成素(Epo)产生细胞。诱导严重贫血以大幅增加Epo的产生。这导致肾脏中Epo mRNA水平升高。小鼠Epo基因的35S标记DNA片段用作原位杂交的探针。并行进行的对照实验包括非贫血小鼠的肾脏、经核糖核酸酶处理的缺氧肾脏切片以及35S标记的非Epo相关DNA。Epo探针在缺氧肾脏的皮质中产生特异性杂交信号,在外髓质中信号较弱。肾小球和肾小管细胞未被标记。所有阳性细胞均被鉴定为肾小管周细胞。通过免疫荧光,我们发现具有相同形态的细胞含有VIII因子相关抗原。这些数据表明,肾小管周细胞,很可能是内皮细胞,是小鼠缺氧肾脏中Epo产生的主要部位。