Glomerular Podocytes Express Protocadherin 17

    • Takata Takuma
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University and Institute for Clinical Research, Niigata National Hospital
    • Yaoita Eishin
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University
    • Kamiie Junichi
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University
    • Li Huiping
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University

    • Yoshida Yutaka
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University
    • Gejyo Fumitake
    • Division of Clinical Nephrology and Rheumatology, Graduate School of Medical and Dental Sciences, Niigata University
    • Yamamoto Tadashi
    • Departmanets of Structural Pathology, Institute of Nephrology, Graduate School of Medical and Dental Sciences, Niigata University

Abstract

During a search for cadherin-related molecules expressed in rat glomeruli by RT-PCR with degenerate primers, we have isolated cDNA encoding protocadherin 17 (Pcdh17) in addition to Fat1. Although Pcdh17 has been suggested to participate in cell-cell adhesion and cell sorting, little is known about its distribution and function. To elucidate the localization and expression of Pcdh17, ribonuclease protection assay and in situ hybridization were performed in the rat. Pcdh17 expression was detected distinctly in RNAs from the cerebrum, cerebellum, lung, but spleen but weakly in RNAs from the whole kidney. In the kidney, intense signals for Pcdh17 were found in glomerular RNAs, with only or weak signals at best in cortical and medullary RNAs. In situ hybridization showed that Pcdh17 was predominantly expressed by podocytes in the glomerulus. Pcdh17 were found to have two isoforms that differ in the length of the cytoplasmic domains. The expression level of both isoforms did not change in puromycin aminonucleoside nephrosis where slit diaphragms disappear and new junctional complexes are newly formed. In conclusion, Pcdh17 is expressed by podocytes, which may be involved in several types of their intercellular junctions.

Journal

Acta medica et biologica   [List of Volumes]

Acta medica et biologica 55(1), 9-15, 2007-03  [Table of Contents]

Niigata University

Codes

  • NII Article ID (NAID) :
    110006447093
  • NII NACSIS-CAT ID (NCID) :
    AA00508361
  • Text Lang :
    ENG
  • ISSN :
    05677734
  • Databases :
    NII-ELS