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Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy.

Publication ,  Journal Article
Ross, MD; Bruggeman, LA; Hanss, B; Sunamoto, M; Marras, D; Klotman, ME; Klotman, PE
Published in: J Biol Chem
August 29, 2003

Growing evidence suggests that human immunodeficiency virus (HIV)-1 infection of podocytes plays a central role in the glomerular disease of HIV-associated nephropathy (HIVAN). As an approach to identify host genes involved in the pathogenesis of the sclerotic glomerular lesion in HIVAN, representational difference analysis of cDNA was used to identify differentially expressed genes in HIV-1 transgenic and nontransgenic podocytes. We isolated a novel member of the small leucine-rich repeat (SLR) protein family, podocan, that is expressed at high levels in the HIV-1 transgenic podocytes. In normal embryonic kidney, a 3.2-kb podocan transcript was detected at low levels, and expression increased dramatically within 24 h following birth. Expression of a 2.3-kb transcript became evident after birth and gradually increased to 50% of the total podocan RNA in the mature kidney. Phylogenetically, podocan represents a new class in the SLR protein gene family, an expanding protein family sharing homology with the small leucine-rich repeat proteoglycans. The 3.2-kb transcript encodes a predicted 611-amino acid secretory protein with 20 leucine-rich repeats, a unique N-terminal cysteine-rich cluster pattern and a highly acidic C-terminal domain. In situ hybridization of normal kidney revealed podocan mRNA expression in podocytes and likely vascular endothelial cells within the glomerulus. The immunohistochemical staining pattern of podocan protein in normal kidney glomeruli was consistent with that of the glomerular basement membrane, and staining was markedly increased in sclerotic glomerular lesions in the transgenic HIVAN model. Thus, podocan defines a new class within the SLR protein family and is a previously unrecognized component of the sclerotic glomerular lesion that develops in the course of experimental HIVAN.

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Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

August 29, 2003

Volume

278

Issue

35

Start / End Page

33248 / 33255

Location

United States

Related Subject Headings

  • Transgenes
  • Time Factors
  • Sequence Homology, Amino Acid
  • RNA, Messenger
  • RNA
  • Proteins
  • Protein Structure, Tertiary
  • Protein Biosynthesis
  • Phylogeny
  • Molecular Sequence Data
 

Citation

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Ross, M. D., Bruggeman, L. A., Hanss, B., Sunamoto, M., Marras, D., Klotman, M. E., & Klotman, P. E. (2003). Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy. J Biol Chem, 278(35), 33248–33255. https://doi.org/10.1074/jbc.M301299200
Ross, Michael D., Leslie A. Bruggeman, Basil Hanss, Masaaki Sunamoto, Daniele Marras, Mary E. Klotman, and Paul E. Klotman. “Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy.J Biol Chem 278, no. 35 (August 29, 2003): 33248–55. https://doi.org/10.1074/jbc.M301299200.
Ross MD, Bruggeman LA, Hanss B, Sunamoto M, Marras D, Klotman ME, et al. Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy. J Biol Chem. 2003 Aug 29;278(35):33248–55.
Ross, Michael D., et al. “Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy.J Biol Chem, vol. 278, no. 35, Aug. 2003, pp. 33248–55. Pubmed, doi:10.1074/jbc.M301299200.
Ross MD, Bruggeman LA, Hanss B, Sunamoto M, Marras D, Klotman ME, Klotman PE. Podocan, a novel small leucine-rich repeat protein expressed in the sclerotic glomerular lesion of experimental HIV-associated nephropathy. J Biol Chem. 2003 Aug 29;278(35):33248–33255.

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

August 29, 2003

Volume

278

Issue

35

Start / End Page

33248 / 33255

Location

United States

Related Subject Headings

  • Transgenes
  • Time Factors
  • Sequence Homology, Amino Acid
  • RNA, Messenger
  • RNA
  • Proteins
  • Protein Structure, Tertiary
  • Protein Biosynthesis
  • Phylogeny
  • Molecular Sequence Data