Literature DB >> 682603

Differentiation of epithelial foot processes and filtration slits: sequential appearance of occluding junctions, epithelial polyanion, and slit membranes in developing glomeruli.

W Reeves, J P Caulfield, M G Farquhar.   

Abstract

The visceral glomerular epithelium of immature glomeruli from newborn rats was examined in order to determine the sequence of events that occurs during differentiation of foot processes and filtration slits. Four different stages of glomerular development were defined: vesicle, S-shaped body, developing capillary loop, and maturing stages. During the vesicle stage, the precursor cells of the glomerular and tubular epithelium are joined by occluding junctions at their apices. During the S-shaped body stage, the tubular and parietal visceral glomerular epithelium differentiate, and the occluding zonulae remain along the presumptive tubule lumen and Bowman's space, respectively. With the appearance of capillary loops the parietal and tubular junctions maintain this arrangement, but the junctions of the visceral epithelium are seen at various levels along the lateral cell margins, suggesting that they migrate along the lateral cell surfaces from apex to base. Initially, broad epithelial processes cover the entire outer aspect of the developing basement membrane. After junctional migration interdigitation of epithelial processes is seen, and the processes are joined by focal occluding junctions (maculae or fasciae). With more elaborate interdigitation, fewer and fewer intercellular spaces are closed by occluding junctions, the junctions become less and less extensive, and normal slit architecture with foot processes bridged by slit membranes predominate. Colloidal iron staining (i.e., epithelial polyanion) is first detected along the lateral epithelial cell surfaces early in the capillary loop stage and becomes concentrated along their basal cell surfaces facing the basement membrane at about the same time as interdigitation is occurring. Therefore, facing the basement membrane at about the same time as interdigitation is occurring. Therefore, sialoproteins appear on the epithelial cell surfaces prior to the development of foot processes and slits. This finding is in keeping with the assumption that epithelial polyanion may be required for development and maintenance of normal foot process and slit organization. Prior to the development of extensive interdigitation, the differentiating glomerular epithelium bears a number of striking similarities to the nephrotic epithelium: foot processes are broad, reduced in number, and often joined by focal occluding junctions; slit diaphragms are reduced in number and displaced away from the basement membrane; and ladder-like structures occur in the filtration slits. The epithelial changes seen in aminonucleoside nephrosis therefore appear to represent a "dedifferentiation" to a more primitive organization, and the events that occur early in this disease process represent a rerun inreverse of events that occur during normal glomerular development.

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Year:  1978        PMID: 682603

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  81 in total

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Authors:  J Meseguer; A García-Ayala; A López-Ruiz; M A Esteban
Journal:  Anat Embryol (Berl)       Date:  1996-04

2.  So-called embryonal hyperplasia of Bowman's capsular epithelium: an immunohistochemical and ultrastructural study.

Authors:  K Ogata; H Hajikano; H Sakaguchi
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

3.  Developmental localization of nephrin in zebrafish and medaka pronephric glomerulus.

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Journal:  J Histochem Cytochem       Date:  2013-01-15       Impact factor: 2.479

4.  Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes.

Authors:  Albrecht G Kramer-Zucker; Stephanie Wiessner; Abbie M Jensen; Iain A Drummond
Journal:  Dev Biol       Date:  2005-09-15       Impact factor: 3.582

5.  Postnatal renal development of rats from mothers that received increased sodium intake.

Authors:  Ana Paula C Balbi; Roberto S Costa; Terezila M Coimbra
Journal:  Pediatr Nephrol       Date:  2004-08-28       Impact factor: 3.714

6.  Nephrin forms a complex with adherens junction proteins and CASK in podocytes and in Madin-Darby canine kidney cells expressing nephrin.

Authors:  Sanna Lehtonen; Eero Lehtonen; Krystyna Kudlicka; Harry Holthöfer; Marilyn G Farquhar
Journal:  Am J Pathol       Date:  2004-09       Impact factor: 4.307

7.  Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development.

Authors:  Yong Kyun Kim; Ido Refaeli; Craig R Brooks; Peifeng Jing; Ramila E Gulieva; Michael R Hughes; Nelly M Cruz; Yannan Liu; Angela J Churchill; Yuliang Wang; Hongxia Fu; Jeffrey W Pippin; Lih Y Lin; Stuart J Shankland; A Wayne Vogl; Kelly M McNagny; Benjamin S Freedman
Journal:  Stem Cells       Date:  2017-09-29       Impact factor: 6.277

8.  Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.

Authors:  Xueping Fan; Qinggang Li; Anna Pisarek-Horowitz; Hila Milo Rasouly; Xiangling Wang; Ramon G Bonegio; Hang Wang; Margaret McLaughlin; Steve Mangos; Raghu Kalluri; Lawrence B Holzman; Iain A Drummond; Dennis Brown; David J Salant; Weining Lu
Journal:  Cell Rep       Date:  2012-07-12       Impact factor: 9.423

9.  Reduced sialylation of podocalyxin--the major sialoprotein of the rat kidney glomerulus--in aminonucleoside nephrosis.

Authors:  D Kerjaschki; A T Vernillo; M G Farquhar
Journal:  Am J Pathol       Date:  1985-03       Impact factor: 4.307

Review 10.  The emergence of the glomerular parietal epithelial cell.

Authors:  Stuart J Shankland; Bart Smeets; Jeffrey W Pippin; Marcus J Moeller
Journal:  Nat Rev Nephrol       Date:  2014-01-28       Impact factor: 28.314

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