Literature DB >> 9742072

Immunohistochemical localization of peroxisomal enzymes in developing rat kidney tissues.

K Johkura1, N Usuda, Y Liang, A Nakazawa.   

Abstract

We studied the developmental changes in the localization of peroxisome-specific enzymes in rat kidney tissues from embryonic Day 16 to postnatal Week 10 by immunoblot analysis and immunohistochemistry, using antibodies for the peroxisomal enzymes catalase, d-amino acid oxidase, l-alpha-hydroxyacid oxidase (isozyme B), and enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase bifunctional protein. Peroxisomal enzymes were detected in the neonatal kidney by immunoblot analysis and their amount increased with kidney development. By light microscopic immunohistochemistry, they were first localized in a few proximal tubules in the juxtamedullary cortex of 18-day embryos. The distribution of proximal tubules positive for them expanded towards the superficial cortex with development. The full thickness of the cortex became positive for the staining by 14 days after birth. Peroxisomes could be detected by electron microscopy in structurally immature proximal tubules in 18-day embryos. Their size increased and the ultrastructure of subcompartments became clear with continuing development of proximal tubules. These results show that peroxisomal enzymes appear in the immature proximal tubules in the kidney of embryos and that the ultrastructure of the peroxisomes and localization of the peroxisomal enzymes develop along with the maturation of proximal tubules and kidney tissues.

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Year:  1998        PMID: 9742072     DOI: 10.1177/002215549804601008

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  4 in total

1.  Use of dual section mRNA in situ hybridisation/immunohistochemistry to clarify gene expression patterns during the early stages of nephron development in the embryo and in the mature nephron of the adult mouse kidney.

Authors:  Kylie Georgas; Bree Rumballe; Lorine Wilkinson; Han Sheng Chiu; Emmanuelle Lesieur; Thierry Gilbert; Melissa H Little
Journal:  Histochem Cell Biol       Date:  2008-07-11       Impact factor: 4.304

2.  Catalase prevents maternal diabetes-induced perinatal programming via the Nrf2-HO-1 defense system.

Authors:  Shiao-Ying Chang; Yun-Wen Chen; Xin-Ping Zhao; Isabelle Chenier; Stella Tran; Alexandre Sauvé; Julie R Ingelfinger; Shao-Ling Zhang
Journal:  Diabetes       Date:  2012-06-25       Impact factor: 9.461

3.  Fasting induces the expression of PGC-1α and ERR isoforms in the outer stripe of the outer medulla (OSOM) of the mouse kidney.

Authors:  Christina T Teng; Yin Li; Pat Stockton; Julie Foley
Journal:  PLoS One       Date:  2011-11-04       Impact factor: 3.240

4.  A high-resolution anatomical ontology of the developing murine genitourinary tract.

Authors:  Melissa H Little; Jane Brennan; Kylie Georgas; Jamie A Davies; Duncan R Davidson; Richard A Baldock; Annemiek Beverdam; John F Bertram; Blanche Capel; Han Sheng Chiu; Dave Clements; Luise Cullen-McEwen; Jean Fleming; Thierry Gilbert; Doris Herzlinger; Derek Houghton; Matt H Kaufman; Elena Kleymenova; Peter A Koopman; Alfor G Lewis; Andrew P McMahon; Cathy L Mendelsohn; Eleanor K Mitchell; Bree A Rumballe; Derina E Sweeney; M Todd Valerius; Gen Yamada; Yiya Yang; Jing Yu
Journal:  Gene Expr Patterns       Date:  2007-03-23       Impact factor: 1.224

  4 in total

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