Kim J, Cha J H, Tisher C C, Madsen K M
Department of Anatomy, Catholic University Medical College, Seoul, Korea.
Am J Physiol. 1996 Apr;270(4 Pt 2):F575-92. doi: 10.1152/ajprenal.1996.270.4.F575.
In the developing rat kidney, both type A and type B intercalated cells are present throughout the medullary collecting duct (MCD), as well as the papillary surface epithelium. After birth, intercalated cells gradually disappear from the papillary surface epithelium and the terminal MCD, and type B cells disappear from the entire MCD. The purpose of this study was to establish the mechanism(s) by which intercalated cells are deleted from the MCD during development. Kidneys from 14-, 16-, 18-, and 20-day-old fetuses and 1-, 3-, 7-, and 14-day-old pups were preserved for light microscopic immunohistochemistry and electron microscopy. Intercalated cells were identified by immunostaining for H(+)-adenosinetriphosphatase (H(+)-ATPase) and band 3 protein. Apoptosis was identified by nick end labeling of DNA fragments, staining with the vital dye toluidine blue, and transmission electron microscopy. Two distinct mechanisms of elimination of intercalated cells were detected. Cells with apical labeling for H(+)-ATPase and basolateral labeling for band 3 protein protruded into the lumen of the MCD as if they were being extruded from the epithelium, and many had lost contact with the basement membrane. Extrusion of the cells with basolateral H(+)-ATPase or with no labeling for H(+)-ATPase was never observed. Apoptosis was observed in the MCD from shortly before birth to 7 days after birth, gradually progressing from the papillary tip toward the outer medulla. Staining for apoptosis was present in H(+)-ATPase-positive apoptotic bodies, located in cells that were negative for H(+)-ATPase. Staining was also occasionally observed in apoptotic cells with basolateral H(+)-ATPase but never in cells with apical H(+)-ATPase. Electron microscopy confirmed the presence of apoptotic intercalated cells in the MCD and demonstrated that apoptotic bodies were located in inner medullary collecting duct (IMCD) cells and principal cells. These results demonstrate that intercalated cells are deleted from the MCD by two distinct mechanisms, one involving apoptosis and subsequent phagocytosis by neighboring principal cells or IMCD cells. Elimination by extrusion affects only type A intercalated cells, whereas deletion by apoptosis appears to occur only in type B intercalated cells.
在发育中的大鼠肾脏中,A型和B型闰细胞存在于整个髓质集合管(MCD)以及乳头表面上皮中。出生后,闰细胞逐渐从乳头表面上皮和终末MCD中消失,B型细胞从整个MCD中消失。本研究的目的是确定在发育过程中闰细胞从MCD中被清除的机制。保存了14、16、18和20日龄胎儿以及1、3、7和14日龄幼崽的肾脏,用于光镜免疫组织化学和电子显微镜检查。通过对H(+)-腺苷三磷酸酶(H(+)-ATP酶)和带3蛋白进行免疫染色来鉴定闰细胞。通过DNA片段缺口末端标记、用活性染料甲苯胺蓝染色以及透射电子显微镜来鉴定细胞凋亡。检测到两种不同的闰细胞清除机制。H(+)-ATP酶顶端标记且带3蛋白基底外侧标记的细胞突入MCD管腔,就好像它们正从上皮中被挤出,并且许多细胞已经与基底膜失去联系。从未观察到具有基底外侧H(+)-ATP酶或无H(+)-ATP酶标记的细胞被挤出。从出生前短时间到出生后7天,在MCD中观察到细胞凋亡,且从乳头尖端逐渐向外髓发展。凋亡染色存在于H(+)-ATP酶阳性的凋亡小体中,这些凋亡小体位于H(+)-ATP酶阴性的细胞中。在具有基底外侧H(+)-ATP酶的凋亡细胞中偶尔也观察到染色,但在具有顶端H(+)-ATP酶的细胞中从未观察到。电子显微镜证实了MCD中存在凋亡的闰细胞,并表明凋亡小体位于内髓集合管(IMCD)细胞和主细胞中。这些结果表明,闰细胞通过两种不同的机制从MCD中被清除,一种机制涉及细胞凋亡以及随后被相邻的主细胞或IMCD细胞吞噬。通过挤出进行的清除仅影响A型闰细胞,而通过凋亡进行的清除似乎仅发生在B型闰细胞中。