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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 |
Sumario: | 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. |
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