Shanks J H, Hill C M, Lappin T R, Maxwell A P
Department of Pathology, Queen's University of Belfast, Royal Group of Hospitals Trust, Northern Ireland, U.K.
J Pathol. 1996 Jul;179(3):283-7. doi: 10.1002/(SICI)1096-9896(199607)179:3<283::AID-PATH594>3.0.CO;2-P.
Erythropoietin (EPO) is the main humoral stimulus of erythropoiesis. In adult mammals, the kidney releases EPO in response to hypoxic stress. Conflicting data have suggested either renal tubular or peritubular cell origins of EPO synthesis in vivo. In situ hybridization studies were performed to define further the kidney cell type(s) capable of increasing EPO gene expression during hypoxic stimulation. EPO gene expression was stimulated in mice exposed to acute hypobaric hypoxia. Kidneys from hypoxic and control normoxic mice were obtained. Six digoxigenin-labelled oligonucleotide probes complementary to EPO exon sequences were utilized for in situ hybridization for EPO messenger RNA. Positive hybridization signals were identified in some proximal tubular cells, confined to the inner third of the renal cortex of hypoxic mouse kidney.
促红细胞生成素(EPO)是红细胞生成的主要体液刺激因子。在成年哺乳动物中,肾脏会在低氧应激时释放EPO。相互矛盾的数据表明,体内EPO合成的细胞起源可能是肾小管细胞或肾小管周围细胞。进行原位杂交研究以进一步确定在低氧刺激期间能够增加EPO基因表达的肾细胞类型。在暴露于急性低压缺氧的小鼠中,EPO基因表达受到刺激。获取了低氧小鼠和对照常氧小鼠的肾脏。使用六个与EPO外显子序列互补的地高辛标记寡核苷酸探针进行EPO信使RNA的原位杂交。在一些近端肾小管细胞中发现了阳性杂交信号,这些细胞局限于低氧小鼠肾脏肾皮质的内三分之一处。