Acute carbon tetrachloride feeding induces damage of large but not small cholangiocytes from BDL rat liver

Author:

LeSage Gene D.1,Glaser Shannon S.2,Marucci Luca3,Benedetti Antonio3,Phinizy Jo Lynne2,Rodgers Rebecca4,Caligiuri Alessandra1,Papa Emanuela1,Tretjak Ziga1,Jezequel Anne-Marie5,Holcomb Leigh A.6,Alpini Gianfranco147

Affiliation:

1. Department of Internal Medicine,

2. Division of Research and Education and

3. Department of Gastroenterology, and

4. Medical Physiology and

5. Institute of Experimental Pathology, University of Ancona, Ancona, Italy 60020

6. Department of Psychiatry and Behavioral Science, Scott & White Hospital and The Texas A&M University System Health Science Center College of Medicine and

7. Central Texas Veterans Health Care System, Temple, Texas 76504; and

Abstract

Bile duct damage and/or loss is limited to a range of duct sizes in cholangiopathies. We tested the hypothesis that CCl4damages only large ducts. CCl4 or mineral oil was given to bile duct-ligated (BDL) rats, and 1, 2, and 7 days later small and large cholangiocytes were purified and evaluated for apoptosis, proliferation, and secretion. In situ, we measured apoptosis by morphometric and TUNEL analysis and the number of small and large ducts by morphometry. Two days after CCl4 administration, we found an increased number of small ducts and reduced number of large ducts. In vitro apoptosis was observed only in large cholangiocytes, and this was accompanied by loss of proliferation and secretion in large cholangiocytes and loss of choleretic effect of secretin. Small cholangiocytes de novo express the secretin receptor gene and secretin-induced cAMP response. Consistent with damage of large ducts, we detected cytochrome P-4502E1 (which CCl4 converts to its radicals) only in large cholangiocytes. CCl4induces selective apoptosis of large ducts associated with loss of large cholangiocyte proliferation and secretion.

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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