Literature DB >> 8967336

Role of apoptotic and nonapoptotic cell death in removal of intercalated cells from developing rat kidney.

J Kim1, J H Cha, C C Tisher, K M Madsen.   

Abstract

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.

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Mesh:

Year:  1996        PMID: 8967336     DOI: 10.1152/ajprenal.1996.270.4.F575

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  14 in total

1.  Interaction with surrounding normal epithelial cells influences signalling pathways and behaviour of Src-transformed cells.

Authors:  Mihoko Kajita; Catherine Hogan; Andrew R Harris; Sophie Dupre-Crochet; Nobue Itasaki; Koichi Kawakami; Guillaume Charras; Masazumi Tada; Yasuyuki Fujita
Journal:  J Cell Sci       Date:  2009-12-21       Impact factor: 5.285

2.  Distinct populations of label-retaining cells in the adult kidney are defined temporally and exhibit divergent regional distributions.

Authors:  Sunil Rangarajan; Bhuvana Sunil; Chunlan Fan; Pei-Xuan Wang; Gary Cutter; Paul W Sanders; Lisa M Curtis
Journal:  Am J Physiol Renal Physiol       Date:  2014-09-18

3.  Expression of ammonia transporter family members, Rh B glycoprotein and Rh C glycoprotein, in the developing rat kidney.

Authors:  Ki-Hwan Han; Su-Youn Lee; Wan-Young Kim; Jung-A Shin; Jin Kim; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2010-04-14

4.  Replication of segment-specific and intercalated cells in the mouse renal collecting system.

Authors:  Philipp Wehrli; Dominique Loffing-Cueni; Brigitte Kaissling; Johannes Loffing
Journal:  Histochem Cell Biol       Date:  2006-12-22       Impact factor: 4.304

5.  Collecting duct-derived cells display mesenchymal stem cell properties and retain selective in vitro and in vivo epithelial capacity.

Authors:  Joan Li; Usukhbayar Ariunbold; Norseha Suhaimi; Nana Sunn; Jinjin Guo; Jill A McMahon; Andrew P McMahon; Melissa Little
Journal:  J Am Soc Nephrol       Date:  2014-06-05       Impact factor: 10.121

6.  Adam10 mediates the choice between principal cells and intercalated cells in the kidney.

Authors:  Qiusha Guo; Yinqiu Wang; Piyush Tripathi; Kalyan R Manda; Malini Mukherjee; Malay Chaklader; Paul F Austin; Kameswaran Surendran; Feng Chen
Journal:  J Am Soc Nephrol       Date:  2014-06-05       Impact factor: 10.121

Review 7.  Regulated acid-base transport in the collecting duct.

Authors:  Carsten A Wagner; Olivier Devuyst; Soline Bourgeois; Nilufar Mohebbi
Journal:  Pflugers Arch       Date:  2009-03-07       Impact factor: 3.657

8.  Plasticity of basal cells during postnatal development in the rat epididymis.

Authors:  Winnie W C Shum; Eric Hill; Dennis Brown; Sylvie Breton
Journal:  Reproduction       Date:  2013-10-01       Impact factor: 3.906

9.  Apoptosis and its related genes in renal epithelial cells of the stone-forming rat.

Authors:  Katsuhito Miyazawa; Koji Suzuki; Ryosuke Ikeda; Manabu T Moriyama; Yoshimichi Ueda; Shogo Katsuda
Journal:  Urol Res       Date:  2004-07-03

10.  Postnatal expression of transport proteins involved in acid-base transport in mouse kidney.

Authors:  Brenda Bonnici; Carsten A Wagner
Journal:  Pflugers Arch       Date:  2004-01-31       Impact factor: 3.657

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