Literature DB >> 26259963

In recurrent primary biliary cirrhosis after liver transplantation, biliary epithelial cells show increased expression of mitochondrial proteins.

Motoko Sasaki1, Maylee Hsu2, Matthew M Yeh2, Yasuni Nakanuma3,4.   

Abstract

In biliary epithelial lesions in primary biliary cirrhosis (PBC), mitochondrial proteins associated with deregulated autophagy are abnormally expressed. We examined whether this could be used as a diagnostic marker for end-stage PBC and recurrent PBC after liver transplantation. We examined the expression of the mitochondrial protein pyruvate dehydrogenase complex-E2 component and cytochrome c oxidase, subunit I (CCO), the autophagy-related marker microtubule-associated protein-light chain 3 (LC3), and p62/sequestosome-1 and the senescence markers p16(Ink4a) and p21(WAF1/Cip1) in small bile ducts and bile ductules in explanted livers from patients with PBC (n = 20) in comparison with liver tissue from control patients (n = 21) and post-transplant samples including recurrent PBC and cellular rejection (n = 28). Intense granular expression of mitochondrial proteins was significantly more frequent in small bile ducts in explanted livers with PBC than in control livers (p < 0.05). Post-transplant samples comprised of three groups: group A (positive for mitochondrial proteins, n = 7), group B (positive for either autophagy-related or senescence markers but negative for mitochondrial proteins, n = 7), and group C (all negative, n = 14). All but one case of group A were clinically and histologically diagnosed as recurrent PBC. In contrast, all cases of group B were diagnosed as cellular rejection. This study suggests that the expression of mitochondrial proteins in small bile ducts may be a useful diagnostic marker for end-stage PBC and recurrent PBC after liver transplantation.

Entities:  

Keywords:  Autophagy and cellular senescence; Biliary epithelial cell; Post-liver transplant rejection; Primary biliary cirrhosis; Pyruvate dehydrogenase complex-E2 component

Mesh:

Substances:

Year:  2015        PMID: 26259963     DOI: 10.1007/s00428-015-1819-3

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  17 in total

1.  Nomenclature of the finer branches of the biliary tree: canals, ductules, and ductular reactions in human livers.

Authors:  Tania A Roskams; Neil D Theise; Charles Balabaud; Govind Bhagat; Prithi S Bhathal; Paulette Bioulac-Sage; Elizabeth M Brunt; James M Crawford; Heather A Crosby; Valeer Desmet; Milton J Finegold; Stephen A Geller; Annette S H Gouw; Prodromos Hytiroglou; A S Knisely; Masamichi Kojiro; Jay H Lefkowitch; Yasuni Nakanuma; John K Olynyk; Young Nyun Park; Bernard Portmann; Romil Saxena; Peter J Scheuer; Alastair J Strain; Swan N Thung; Ian R Wanless; A Brian West
Journal:  Hepatology       Date:  2004-06       Impact factor: 17.425

Review 2.  Primary biliary cirrhosis.

Authors:  Marshall M Kaplan; M Eric Gershwin
Journal:  N Engl J Med       Date:  2005-09-22       Impact factor: 91.245

3.  Primary biliary cirrhosis.

Authors:  Keith D Lindor; M Eric Gershwin; Raoul Poupon; Marshall Kaplan; Nora V Bergasa; E Jenny Heathcote
Journal:  Hepatology       Date:  2009-07       Impact factor: 17.425

4.  Immunohistochemical evidence of disease recurrence after liver transplantation for primary biliary cirrhosis.

Authors:  J Van de Water; L B Gerson; L D Ferrell; J R Lake; R L Coppel; K P Batts; R H Wiesner; M E Gershwin
Journal:  Hepatology       Date:  1996-11       Impact factor: 17.425

5.  Autophagy mediates the process of cellular senescence characterizing bile duct damages in primary biliary cirrhosis.

Authors:  Motoko Sasaki; Masami Miyakoshi; Yasunori Sato; Yasuni Nakanuma
Journal:  Lab Invest       Date:  2010-03-08       Impact factor: 5.662

6.  Hepatic distribution of E2 component of pyruvate dehydrogenase complex after transplantation.

Authors:  J Neuberger; L Wallace; R Joplin; S Hubscher
Journal:  Hepatology       Date:  1995-09       Impact factor: 17.425

7.  Replicative senescence of biliary epithelial cells precedes bile duct loss in chronic liver allograft rejection: increased expression of p21(WAF1/Cip1) as a disease marker and the influence of immunosuppressive drugs.

Authors:  J G Lunz; S Contrucci; K Ruppert; N Murase; J J Fung; T E Starzl; A J Demetris
Journal:  Am J Pathol       Date:  2001-04       Impact factor: 4.307

8.  Frequent cellular senescence in small bile ducts in primary biliary cirrhosis: a possible role in bile duct loss.

Authors:  Motoko Sasaki; Hiroko Ikeda; Hironori Haga; Toshiaki Manabe; Yasuni Nakanuma
Journal:  J Pathol       Date:  2005-03       Impact factor: 7.996

9.  Biliary epithelial-mesenchymal transition in posttransplantation recurrence of primary biliary cirrhosis.

Authors:  Helen Robertson; John A Kirby; William W Yip; David E J Jones; Alastair D Burt
Journal:  Hepatology       Date:  2007-04       Impact factor: 17.425

10.  Biliary epithelial senescence and plasticity in acute cellular rejection.

Authors:  J G Brain; H Robertson; E Thompson; E H Humphreys; A Gardner; T A Booth; D E J Jones; S C Afford; T von Zglinicki; A D Burt; J A Kirby
Journal:  Am J Transplant       Date:  2013-06-10       Impact factor: 8.086

View more
  2 in total

1.  Externalization of Mitochondrial PDCE2 on Irradiated Endothelium as a Target for Radiation-Guided Drug Delivery and Precision Thrombosis of Pathological Vasculature.

Authors:  Fahimeh Faqihi; Marcus A Stoodley; Lucinda S McRobb
Journal:  Int J Mol Sci       Date:  2022-08-10       Impact factor: 6.208

Review 2.  Recent advances in the diagnosis and treatment of primary biliary cholangitis.

Authors:  Ying-Qiu Huang
Journal:  World J Hepatol       Date:  2016-11-28
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.