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IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration
AIMS: To investigate the role and the regulation of the long variant of myeloid cell leukemia-1 protein (Mcl-1(L)) during liver regeneration. BACKGROUND: Liver regeneration is an important phenomenon after liver injury. The rat partial hepatectomy (PH) model was used to characterize liver regenerati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692501/ https://www.ncbi.nlm.nih.gov/pubmed/23825534 http://dx.doi.org/10.1371/journal.pone.0066268 |
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author | Chou, Chia-Hung Lai, Shuo-Lun Chen, Chiung-Nien Lee, Po-Huang Peng, Fu-Chuo Kuo, Min-Liang Lai, Hong-Shiee |
author_facet | Chou, Chia-Hung Lai, Shuo-Lun Chen, Chiung-Nien Lee, Po-Huang Peng, Fu-Chuo Kuo, Min-Liang Lai, Hong-Shiee |
author_sort | Chou, Chia-Hung |
collection | PubMed |
description | AIMS: To investigate the role and the regulation of the long variant of myeloid cell leukemia-1 protein (Mcl-1(L)) during liver regeneration. BACKGROUND: Liver regeneration is an important phenomenon after liver injury. The rat partial hepatectomy (PH) model was used to characterize liver regeneration and Mcl-1L expression after PH. METHODS: Male Wistar rats were subjected to 70% PH. The expression of mcl-1L mRNA was determined by quantitative RT-PCR, and protein levels were analyzed by Western blot analysis and immunohistochemistry during liver regeneration. Functional evaluations of Mcl-1(L) were tested using chemical inhibition (flavopiridol), genetic inhibition (siRNA) of Mcl-1L production, and by assaying for annexin V levels and DNA ladder formation. Serum IL-6 levels were determined by enzyme immunoassays; signal transduction of IL-6-regulated Mcl-1L expression was verified by chemical inhibitors and decoy double-stranded oligodeoxynucleotides. RESULTS: High levels of Mcl-1(L) were observed in remnant tissue at 4 h after PH. Administration of flavopiridol decreased Mcl-1(L) accumulation and also inhibited liver regeneration. IL-6 administration promoted the accumulation of Mcl-1(L) in rat hepatocytes, an effect that was impaired by siRNA treatments that reduced Mcl-1(L) production. Chemical inhibition and decoy oligonucleotide competition demonstrated that IL-6-induced Mcl-1(L) production required signaling mediated by JAK kinase, phosphoinositide 3-kinase (PI3K), and cAMP response-element-binding (CREB) proteins. CONCLUSION: Mcl-1(L) is an anti-apoptotic protein induced during liver regeneration after PH in rats. The expression of Mcl-1(L) is induced by IL-6 through the JAK/PI3K/Akt/CREB signaling pathway. Chemotherapy drugs that depend on Mcl-1(L)- or IL-6-related signaling should be considered carefully before use in patients undergoing hepatectomy for malignant tumor resection. |
format | Online Article Text |
id | pubmed-3692501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36925012013-07-02 IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration Chou, Chia-Hung Lai, Shuo-Lun Chen, Chiung-Nien Lee, Po-Huang Peng, Fu-Chuo Kuo, Min-Liang Lai, Hong-Shiee PLoS One Research Article AIMS: To investigate the role and the regulation of the long variant of myeloid cell leukemia-1 protein (Mcl-1(L)) during liver regeneration. BACKGROUND: Liver regeneration is an important phenomenon after liver injury. The rat partial hepatectomy (PH) model was used to characterize liver regeneration and Mcl-1L expression after PH. METHODS: Male Wistar rats were subjected to 70% PH. The expression of mcl-1L mRNA was determined by quantitative RT-PCR, and protein levels were analyzed by Western blot analysis and immunohistochemistry during liver regeneration. Functional evaluations of Mcl-1(L) were tested using chemical inhibition (flavopiridol), genetic inhibition (siRNA) of Mcl-1L production, and by assaying for annexin V levels and DNA ladder formation. Serum IL-6 levels were determined by enzyme immunoassays; signal transduction of IL-6-regulated Mcl-1L expression was verified by chemical inhibitors and decoy double-stranded oligodeoxynucleotides. RESULTS: High levels of Mcl-1(L) were observed in remnant tissue at 4 h after PH. Administration of flavopiridol decreased Mcl-1(L) accumulation and also inhibited liver regeneration. IL-6 administration promoted the accumulation of Mcl-1(L) in rat hepatocytes, an effect that was impaired by siRNA treatments that reduced Mcl-1(L) production. Chemical inhibition and decoy oligonucleotide competition demonstrated that IL-6-induced Mcl-1(L) production required signaling mediated by JAK kinase, phosphoinositide 3-kinase (PI3K), and cAMP response-element-binding (CREB) proteins. CONCLUSION: Mcl-1(L) is an anti-apoptotic protein induced during liver regeneration after PH in rats. The expression of Mcl-1(L) is induced by IL-6 through the JAK/PI3K/Akt/CREB signaling pathway. Chemotherapy drugs that depend on Mcl-1(L)- or IL-6-related signaling should be considered carefully before use in patients undergoing hepatectomy for malignant tumor resection. Public Library of Science 2013-06-25 /pmc/articles/PMC3692501/ /pubmed/23825534 http://dx.doi.org/10.1371/journal.pone.0066268 Text en © 2013 Chou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chou, Chia-Hung Lai, Shuo-Lun Chen, Chiung-Nien Lee, Po-Huang Peng, Fu-Chuo Kuo, Min-Liang Lai, Hong-Shiee IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title | IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title_full | IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title_fullStr | IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title_full_unstemmed | IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title_short | IL-6 Regulates Mcl-(1L) Expression through the JAK/PI3K/Akt/CREB Signaling Pathway in Hepatocytes: Implication of an Anti-Apoptotic Role during Liver Regeneration |
title_sort | il-6 regulates mcl-(1l) expression through the jak/pi3k/akt/creb signaling pathway in hepatocytes: implication of an anti-apoptotic role during liver regeneration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692501/ https://www.ncbi.nlm.nih.gov/pubmed/23825534 http://dx.doi.org/10.1371/journal.pone.0066268 |
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