Fusion of proinsulin-producing bone marrow-derived cells with hepatocytes in diabetes

  1. Mineko Fujimiya*,,
  2. Hideto Kojima,,
  3. Masumi Ichinose*,
  4. Ryohachi Arai*,
  5. Hiroshi Kimura,
  6. Atsunori Kashiwagi§, and
  7. Lawrence Chan,
  1. Departments of *Anatomy,
  2. Molecular Genetics in Medicine, and
  3. §Medicine, Section of Endocrinology and Metabolism, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan; and
  4. Division of Diabetes, Endocrinology, and Metabolism, Departments of Medicine and Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030
  1. Communicated by Salih J. Wakil, Baylor College of Medicine, Houston, TX, January 9, 2007 (received for review November 6, 2006)

Abstract

We previously reported that diabetes in mice is associated with the appearance of proinsulin-producing (Proins-P) cells in the liver. It was unclear, however, whether these Proins-P bone marrow-derived cells (BMDC) merely transit through the liver or undergo fusion with hepatocytes, normally an extremely rare event. In this study, we found that, in diabetes, BMDC in the liver produce not only Proins but also TNF-α, suggesting that diabetes reprograms gene expression in BMDC, turning on “inappropriate” genes. Bone marrow transplantation using genetically marked donor and recipient mice showed that fusion occurs between Proins-P BMDC and hepatocytes. Cell fusion is further supported by the presence of the Y chromosome in Proins-P cells in female mice that received male bone marrow transplantation cells. Morphologically, Proins-P fusion cells are albumin-producing hepatocytes that constitute ≈2.5% of the liver section area 5 months after diabetes induction. An extensive search failed to reveal any fusion cells in nondiabetic mice. Thus, diabetes causes fusion between Proins-P BMDC and hepatocytes in vivo, an observation that has implications for the pathophysiology of diabetes as well as the fundamental biology of heterotypic cell fusion.

Footnotes

  • To whom correspondence should be addressed. E-mail: lchan{at}bcm.edu
  • Author contributions: M.F. and H. Kojima contributed equally to this work; M.F., H. Kojima, and L.C. designed research; M.F., H. Kojima, and M.I. performed research; R.A., H. Kimura, and A.K. contributed new reagents/analytic tools; M.F., H. Kojima, and L.C. analyzed data; and M.F., H. Kojima, and L.C. wrote the paper.

  • The authors declare no conflict of interest.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0700220104/DC1.

  • Abbreviations:
    BMDC,
    bone marrow-derived cells;
    BMT,
    bone marrow transplantation;
    Proins-P,
    proinsulin-producing;
    STZ,
    streptozotocin.
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