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Bag-1L Protects against Cell Apoptosis in an In Vitro Model of Lung Ischemia-Reperfusion Injury through the C-Terminal "Bag" Domain.
Lv, Ji-Ling; Shi, Li-Na; Zhai, Cong-Ying; Wang, Ge-Jin; Qu, Yan.
Afiliación
  • Lv JL; Department of Respiratory Medicine, Shandong Second Provincial General Hospital, Jinan, 250000 Shandong, China.
  • Shi LN; Department of Intensive Care Unit, Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao, 266071 Shandong, China.
  • Zhai CY; Zibo Traditional Chinese Medicine Hospital, Zibo, 255200 Shandong, China.
  • Wang GJ; Department of Respiratory Medicine, The First Hospital of Zibo, Zibo, 255200 Shandong, China.
  • Qu Y; Affiliated Hospital of Zibo Vocational Institute, Zibo, 255314 Shandong, China.
Biomed Res Int ; 2021: 8822807, 2021.
Article en En | MEDLINE | ID: mdl-34056003
ABSTRACT
Bcl-2-associated athanogene 1 (Bag-1) is a multifunctional and antiapoptotic protein that binds to the antiapoptosis regulator Bcl-2 and promotes cell survival. To investigate the protective function of Bag-1, we examined the effects of Bag-1L, one isoform of Bag-1, in an in vitro cell culture model of lung ischemia-reperfusion injury (LIRI) generated by treatment of A549 cells with hypoxia/reoxygenation. Overexpression of full-length Bag-1L increased the viability of A549 cells and reduced cell apoptosis in response to 6 h of hypoxia/reoxygenation treatment. Furthermore, Bag-1L overexpression enhanced the heat shock protein 70 (HSP70) and Bcl-2 protein levels, increased the phosphorylation of AKT, decreased Bax and cleaved caspase-3 levels, and was able to overcome cell cycle arrest. These effects were not observed in A549 cells overexpressing a truncated form of Bag-1L lacking the "Bag domain," denoted Bag-1L△C. The "Bag domain" is the C-terminal 47 amino acids. Taken together, the results of this study suggest that Bag-1L overexpression can protect against oxidative stress and apoptosis in an in vitro LIRI model, with a dependence on the Bag domain.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Daño por Reperfusión / Apoptosis / Sustancias Protectoras / Proteínas de Unión al ADN / Pulmón Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Daño por Reperfusión / Apoptosis / Sustancias Protectoras / Proteínas de Unión al ADN / Pulmón Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biomed Res Int Año: 2021 Tipo del documento: Article País de afiliación: China