Gu Qiang, Xiao Ying-Bin, Wang Yong
Department of Cardiovascular Surgery, Xinqiao Hospital, Second Affiliated Hospital of Army Military Medical University, No.183 Xinqiao Street, Shapingba District, Chongqing, 400037, China.
Vascular Injury and Repair Laboratory, Xinqiao Hospital, Second Affiliated Hospital of Army Medical University, Chongqing, 400037, China.
J Physiol Biochem. 2024 Feb;80(1):127-136. doi: 10.1007/s13105-023-00989-7. Epub 2023 Oct 19.
Suppressor of cytokine signaling 3 (SOCS3) plays a significant role in the process of myocardial adaptation to chronic hypoxia. SOCS3 finely regulates cell signaling cross-talk that occurs between NF-κB and STAT3 during the compensatory protective response. However, the role and mechanism of SOCS3 in hypoxic cardiomyocytes are not fully understood. In the study, we investigated the effect of SOCS3 on the p65 and STAT3 signaling pathways and further examined the potential molecular mechanism involved in regulating apoptosis. Our data showed that SOCS3 silencing could upregulate Ac-p65, p-p65, and p-STAT3 expression in nuclear extracts of H9c2 cells that received hypoxic treatment for 24, 48, and 72 h. SOCS3 silencing also remarkably increased the DNA-binding activity of the p65 motif in hypoxic cultivated H9c2 cells. We also found that SOCS3 knockdown increased cleaved-caspase-3, Bax, and PUMA expression and decreased cleaved PARP and Bcl-2 in expression in hypoxic H9c2 cells. Silencing of SOCS3 caused an increase in LDH leakage from injured cardiomyocytes and reduced cell viability under conditions of hypoxic stress. Furthermore, SOCS3 silencing enhanced the apoptosis of H9c2 cells at 72 h of hypoxia. These findings suggest that knockdown of SOCS3 leads to excessive activation of the NF-κB pathway, which, in turn, might promote apoptosis under conditions of chronic hypoxia.
细胞因子信号转导抑制因子3(SOCS3)在心肌适应慢性缺氧的过程中发挥着重要作用。在代偿性保护反应过程中,SOCS3精细调节NF-κB与STAT3之间发生的细胞信号串扰。然而,SOCS3在缺氧心肌细胞中的作用和机制尚未完全明确。在本研究中,我们探究了SOCS3对p65和STAT3信号通路的影响,并进一步研究了其调控细胞凋亡的潜在分子机制。我们的数据显示,在接受24、48和72小时缺氧处理的H9c2细胞的核提取物中,沉默SOCS3可上调乙酰化p65(Ac-p65)、磷酸化p65(p-p65)和磷酸化STAT3(p-STAT3)的表达。沉默SOCS3还显著增加了缺氧培养的H9c2细胞中p65基序的DNA结合活性。我们还发现,在缺氧的H9c2细胞中,敲低SOCS3可增加裂解型半胱天冬酶-3(cleaved-caspase-3)、Bax和PUMA的表达,并降低裂解型聚(ADP-核糖)聚合酶(cleaved PARP)和Bcl-2的表达。沉默SOCS3导致受损心肌细胞的乳酸脱氢酶(LDH)泄漏增加,并在缺氧应激条件下降低细胞活力。此外,在缺氧72小时时,沉默SOCS3增强了H9c2细胞的凋亡。这些发现表明,敲低SOCS3会导致NF-κB通路过度激活,进而可能在慢性缺氧条件下促进细胞凋亡。