Literature DB >> 22694592

Amphiregulin stimulates liver regeneration after small-for-size mouse liver transplantation.

Q Liu1, H Rehman, Y Krishnasamy, K Haque, R G Schnellmann, J J Lemasters, Z Zhong.   

Abstract

This study investigated whether amphiregulin (AR), a ligand of the epidermal growth factor receptor (EGFR), improves liver regeneration after small-for-size liver transplantation. Livers of male C57BL/6 mice were reduced to ~50% and ~30% of original sizes and transplanted. After transplantation, AR and AR mRNA increased in 50% but not in 30% grafts. 5-Bromodeoxyuridine (BrdU) labeling, proliferating cell nuclear antigen (PCNA) expression and mitotic index increased substantially in 50% but not 30% grafts. Hyperbilirubinemia and hypoalbuminemia occurred and survival decreased after transplantation of 30% but not 50% grafts. AR neutralizing antibody blunted regeneration in 50% grafts whereas AR injection (5 μg/mouse, iv) stimulated liver regeneration, improved liver function and increased survival after transplantation of 30% grafts. Phosphorylation of EGFR and its downstream signaling molecules Akt, mTOR, p70S6K, ERK and JNK increased markedly in 50% but not 30% grafts. AR stimulated EGFR phosphorylation and its downstream signaling pathways. EGFR inhibitor PD153035 suppressed regeneration of 50% grafts and largely abrogated stimulation of regeneration of 30% grafts by AR. AR also increased cyclin D1 and cyclin E expression in 30% grafts. Together, liver regeneration is suppressed in small-for-size grafts, as least in part, due to decreased AR formation. AR supplementation could be a promising therapy to stimulate regeneration of partial liver grafts. © Copyright 2012 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Year:  2012        PMID: 22694592      PMCID: PMC3409348          DOI: 10.1111/j.1600-6143.2012.04069.x

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  64 in total

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3.  Ischemic preconditioning prevents free radical production and mitochondrial depolarization in small-for-size rat liver grafts.

Authors:  Hasibur Rehman; Henry D Connor; Venkat K Ramshesh; Tom P Theruvath; Ronald P Mason; Gary L Wright; John J Lemasters; Zhi Zhong
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4.  Transient expression of cyclin D1 is sufficient to promote hepatocyte replication and liver growth in vivo.

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5.  Mammalian TOR: a homeostatic ATP sensor.

Authors:  P B Dennis; A Jaeschke; M Saitoh; B Fowler; S C Kozma; G Thomas
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Review 8.  Amphiregulin: a new growth factor in hepatocarcinogenesis.

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Authors:  Z Zhong; T P Theruvath; R T Currin; P C Waldmeier; J J Lemasters
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Review 6.  EGFR Signaling in Liver Diseases.

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7.  Dickkopf-1 and Amphiregulin as Novel Biomarkers and Potential Therapeutic Targets in Hepatocellular Carcinoma.

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8.  The mitochondria-targeted antioxidant MitoQ attenuates liver fibrosis in mice.

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9.  Suppression of graft regeneration, not ischemia/reperfusion injury, is the primary cause of small-for-size syndrome after partial liver transplantation in mice.

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10.  Amphiregulin activates regulatory T lymphocytes and suppresses CD8+ T cell-mediated anti-tumor response in hepatocellular carcinoma cells.

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