Literature DB >> 15350473

Correlation of cell necrosis and tissue calcification with ischemia/reperfusion injury after liver transplantation.

G N Tzimas1, M Afshar, A Emadali, E Chevet, H Vali, P P Metrakos.   

Abstract

BACKGROUND: The cellular events following liver ischemia/reperfusion (I/R) during transplantation are largely unknown. The spectrum of I/R damage to the liver can be clinically revealed by the development of primary graft dysfunction or nonfunction. Because viral-induced liver necrosis has been associated with the development of calcifications in an animal model, we investigated the spectrum of I/R changes identified at an ultrastructural level among livers after liver transplant (LT).
MATERIALS AND METHODS: Random liver biopsies from five recipients with different degrees of liver dysfunction (LD) were processed for light (LM) and electron (EM) microscopic examination. The degree of calcification was estimated as mild-moderate or severe. The degree of cell vacuolization, used as a surrogate marker of cell necrosis, was reported as mild-moderate or severe.
RESULTS: Two patients with severe LD had obvious calcifications by LM and EM examinations. Both showed significant vacuole formation, suggesting a severe degree of cell necrosis, and both succumbed to the sequelae of their LD. One patient showed evidence of mild calcifications at EM (but not LM) examination, with mild vacuole formation. The remaining two patients displayed no microcalcifications. Both presented only mild vacuole formation. Both patients recovered from LD and are currently alive.
CONCLUSION: In this preliminary report, we conclude that the clinically observed degree of LD after orthotopic liver transplant (OLT)correlates well with ultrastructural modifications. These include calcification and vacuole formation. We believe that both findings can be used as surrogate markers of a clinically significant hepatic I/R injury.

Entities:  

Mesh:

Year:  2004        PMID: 15350473     DOI: 10.1016/j.transproceed.2004.06.013

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  6 in total

Review 1.  The Mechanism and Regulation of the NLRP3 Inflammasome during Fibrosis.

Authors:  Carol M Artlett
Journal:  Biomolecules       Date:  2022-04-26

Review 2.  Apoptosis and necroptosis in the liver: a matter of life and death.

Authors:  Robert F Schwabe; Tom Luedde
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2018-12       Impact factor: 46.802

3.  Extracellular Ca2+ is a danger signal activating the NLRP3 inflammasome through G protein-coupled calcium sensing receptors.

Authors:  Manuela Rossol; Matthias Pierer; Nora Raulien; Dagmar Quandt; Undine Meusch; Kathrin Rothe; Kristin Schubert; Torsten Schöneberg; Michael Schaefer; Ute Krügel; Sanela Smajilovic; Hans Bräuner-Osborne; Christoph Baerwald; Ulf Wagner
Journal:  Nat Commun       Date:  2012       Impact factor: 14.919

4.  A novel atheroprotective role of MF59-like adjuvant when co-administered with CETP vaccine in rabbit model of atherosclerosis.

Authors:  Tamara Aghebati; Amir Hooshang Mohammadpour; Mohammad Afshar; Mahmoud Reza Jaafari; Khalil Abnous; Saeed Nazemi; Sobhan Issazadeh; Saeed Hashemzadeh; Mohammad Zare; Ali Badiee
Journal:  Iran J Basic Med Sci       Date:  2016-12       Impact factor: 2.699

5.  Quantitative chemical imaging of breast calcifications in association with neoplastic processes.

Authors:  Kseniya S Shin; Mint Laohajaratsang; Shuaiqian Men; Benjamin Figueroa; Suzanne M Dintzis; Dan Fu
Journal:  Theranostics       Date:  2020-04-27       Impact factor: 11.556

6.  Early graft calcification without graft dysfunction after living donor liver transplantation: two case reports.

Authors:  Peilin Li; Masaaki Hidaka; Yu Huang; Takanobu Hara; Kantoku Nagakawa; Hajime Matsushima; Takayuki Tanaka; Tomohiko Adachi; Akihiko Soyama; Weili Gu; Kengo Kanetaka; Susumu Eguchi
Journal:  Clin J Gastroenterol       Date:  2021-08-22
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.