Literature DB >> 8785396

Identification of distinct subpopulations of intercalated cells in the mouse collecting duct.

P Teng-umnuay1, J W Verlander, W Yuan, C C Tisher, K M Madsen.   

Abstract

Structurally and functionally distinct populations of intercalated cells have been described in the collecting duct of both rat and rabbit. However, little is known about these cells in the mouse kidney. The study presented here examines ultrastructural and immunological characteristics of different types of intercalated cells in the mouse. Kidneys of two strains of normal female mice, C57BL/6 and IBR, were preserved by in vivo perfusion with 1% glutaraldehyde or paraformaldehyde-picric acid fixatives and processed for morphological evaluation or light and electron microscopic immunohistochemistry, respectively. The avidin-biotin-horseradish peroxidase procedure was performed on was sections using antibodies against carbonic anhydrase II, H+ -ATPase and Band 3 protein. Immunogold cytochemistry was performed on Lowicryl sections using antibodies to H+ -ATPase and Band 3 protein. Colocalization of H+ -ATPase and Band 3 protein was performed by double labeling using an immunogold technique with silver enhancement. Intercalated cells identified by positive staining for H+ -ATPase and carbonic anhydrase II constituted 35% to 40% of all cells in the connecting tubule (CNT), cortical collecting duct (CCD), and outer medullary collecting duct (OMCD). Type A intercalated cells identified by positive Band 3 staining constituted 16%, 24%, and 33% of the total cell population in the CNT, CCD, and OMCD, respectively. Electron microscopy and immunogold cytochemistry demonstrated three distinct populations of intercalated cells. Type A intercalated cells with apical H+ -ATPase and basolateral Band 3 immunoreactivity were present in all segments examined, and had prominent apical microprojections and characteristic tubulovesicular structures beneath the apical surface, both coated with studs on the cytoplasmic face. Type B intercalated cells with basolateral and cytoplasmic H+-ATPase and no Band 3 immunoreactivity were most frequently observed in the initial collecting tubule, but were present also in the CNT and early CCD. Type B intercalated cells had a fairly smooth apical surface, a gray zone free of organelles beneath the apical plasma membrane, and small cytoplasmic vesicles without studs throughout the cell. A third type of intercalated cell with apical and cytoplasmic H+-ATPase, but no basolateral Band 3 protein, was observed exclusively in the CNT and the initial collecting tubule. This type of cell was large, with numerous mitochondria, and vesicles coated with studs were present throughout the cell. It resembled a third type of intercalated cell described previously in the rat. It is concluded that three morphologically and immunologically distinct types of intercalated cells are present in the mouse kidney.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8785396     DOI: 10.1681/ASN.V72260

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  35 in total

1.  Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.

Authors:  I E Royaux; S M Wall; L P Karniski; L A Everett; K Suzuki; M A Knepper; E D Green
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

2.  Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1.

Authors:  Sandra Rodrigo Blomqvist; Hilmar Vidarsson; Sharyn Fitzgerald; Bengt R Johansson; Anna Ollerstam; Russell Brown; A Erik G Persson; G öran Bergström G; Sven Enerbäck
Journal:  J Clin Invest       Date:  2004-06       Impact factor: 14.808

3.  Angiotensin II stimulates H⁺-ATPase activity in intercalated cells from isolated mouse connecting tubules and cortical collecting ducts.

Authors:  Carsten A Wagner; Nilufar Mohebbi; Ulrike Uhlig; Gerhard H Giebisch; Sylvie Breton; Dennis Brown; John P Geibel
Journal:  Cell Physiol Biochem       Date:  2011-11-18

4.  Remodeling of the fetal collecting duct epithelium.

Authors:  Michael J Hiatt; Larissa Ivanova; Nuria Toran; Alice F Tarantal; Douglas G Matsell
Journal:  Am J Pathol       Date:  2009-12-24       Impact factor: 4.307

5.  MiRP3 acts as an accessory subunit with the BK potassium channel.

Authors:  Daniel I Levy; Sherry Wanderling; Daniel Biemesderfer; Steve A N Goldstein
Journal:  Am J Physiol Renal Physiol       Date:  2008-05-07

6.  Site-specific expression of IQGAP1, a key mediator of cytoskeleton, in mouse renal tubules.

Authors:  Li-Wen Lai; Kim-Chong Yong; Yeong-Hau H Lien
Journal:  J Histochem Cytochem       Date:  2008-04-14       Impact factor: 2.479

Review 7.  A new look at electrolyte transport in the distal tubule.

Authors:  Dominique Eladari; Régine Chambrey; Janos Peti-Peterdi
Journal:  Annu Rev Physiol       Date:  2011-09-02       Impact factor: 19.318

Review 8.  Molecular mechanisms and regulation of urinary acidification.

Authors:  Ira Kurtz
Journal:  Compr Physiol       Date:  2014-10       Impact factor: 9.090

9.  Endogenous Notch Signaling in Adult Kidneys Maintains Segment-Specific Epithelial Cell Types of the Distal Tubules and Collecting Ducts to Ensure Water Homeostasis.

Authors:  Malini Mukherjee; Jennifer deRiso; Karla Otterpohl; Ishara Ratnayake; Divya Kota; Phil Ahrenkiel; Indra Chandrasekar; Kameswaran Surendran
Journal:  J Am Soc Nephrol       Date:  2018-12-04       Impact factor: 10.121

10.  Inactivation of Pkd1 in principal cells causes a more severe cystic kidney disease than in intercalated cells.

Authors:  Kalani L Raphael; Kevin A Strait; Peter K Stricklett; R Lance Miller; Raoul D Nelson; Klaus B Piontek; Gregory G Germino; Donald E Kohan
Journal:  Kidney Int       Date:  2009-01-14       Impact factor: 10.612

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.