Cytoglobin/STAP, its unique localization in splanchnic fibroblast-like cells and function in organ fibrogenesis

Lab Invest. 2004 Jan;84(1):91-101. doi: 10.1038/labinvest.3700013.

Abstract

Cytoglobin/stellate cell activation-associated protein (Cygb/STAP) consists of a new class of hexacoordinate globin superfamily, which was recently discovered by a proteome analysis on the rat hepatic stellate cells. Unlike haemoglobin, myoglobin, and neuroglobin, Cygb/STAP is ubiquitously expressed in several organs, although its detailed localization has not been clarified. Immunohistochemistry and immunoelectron microscopy revealed that Cygb/STAP is uniquely localized in fibroblast-like cells in splanchnic organs, namely the vitamin A-storing cell lineage, but neither in epithelial cells, endothelial cells, muscle cells, blood cells, macrophages, nor dermal fibroblasts. The expression of Cygb/STAP was upregulated in fibrotic lesions of the pancreas and kidney in which activated fibroblast-like cells or myofibroblasts are known to increase in number. In cultured hepatic stellate cells, Cygb/STAP expression was augmented by the stimulation with sera, platelet-derived growth factor-BB, and transforming growth factor-beta 1. Overexpression of Cygb/STAP in NIH 3T3 cells induced the cells to lessen migratory activities and increase the expression of collagen alpha1(I) mRNA. These results indicate that Cygb/STAP is a tissue globin uniquely localized in splanchnic fibroblastic cell lineage and may play a role in fibrotic organ disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Becaplermin
  • Biomarkers / analysis
  • Chronic Disease
  • Collagen Type I / genetics
  • Collagen Type I / metabolism
  • Cytoglobin
  • Disease Models, Animal
  • Fibrosis / chemically induced
  • Fibrosis / enzymology*
  • Fibrosis / pathology
  • Fluorescent Antibody Technique, Indirect
  • Globins / analysis
  • Globins / metabolism*
  • Hemeproteins / analysis
  • Hemeproteins / metabolism*
  • Kidney Diseases / chemically induced
  • Kidney Diseases / enzymology
  • Kidney Diseases / pathology
  • Kupffer Cells / drug effects
  • Kupffer Cells / enzymology
  • Kupffer Cells / ultrastructure
  • Male
  • Mice
  • NIH 3T3 Cells / drug effects
  • NIH 3T3 Cells / enzymology*
  • NIH 3T3 Cells / ultrastructure
  • Pancreas / enzymology
  • Pancreas / pathology
  • Pancreatitis / enzymology
  • Pancreatitis / etiology
  • Pancreatitis / pathology
  • Peroxidases / analysis
  • Peroxidases / metabolism*
  • Platelet-Derived Growth Factor / pharmacology
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Specific Pathogen-Free Organisms
  • Transfection
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta1
  • Vitamin A / analysis
  • Vitamin A / metabolism

Substances

  • Biomarkers
  • Collagen Type I
  • Cygb protein, rat
  • Cytoglobin
  • Hemeproteins
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger
  • Tgfb1 protein, mouse
  • Tgfb1 protein, rat
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Vitamin A
  • Becaplermin
  • Globins
  • Peroxidases