Roufayel Rabih, Younes Khaled, Al-Sabi Ahmed, Murshid Nimer
College of Engineering and Technology, American University of the Middle East, Kuwait.
Life (Basel). 2022 Feb 9;12(2):256. doi: 10.3390/life12020256.
Apoptosis is an evolutionarily conserved and tightly regulated cell death pathway. Physiological cell death is important for maintaining homeostasis and optimal biological conditions by continuous elimination of undesired or superfluous cells. The BH3-only pro-apoptotic members are strong inducers of apoptosis. The pro-apoptotic BH3-only protein Noxa activates multiple death pathways by inhibiting the anti-apoptotic Bcl-2 family protein, Mcl-1, and other protein members leading to Bax and Bak activation and MOMP. On the other hand, Puma is induced by p53-dependent and p53-independent apoptotic stimuli in several cancer cell lines. Moreover, this protein is involved in several physiological and pathological processes, such as immunity, cancer, and neurodegenerative diseases. Future heat shock research could disclose the effect of hyperthermia on both Noxa and BH3-only proteins. This suggests post-transcriptional mechanisms controlling the translation of both Puma and Noxa mRNA in heat-shocked cells. This study was also the chance to recapitulate the different reactional mechanisms investigated for caspases.
细胞凋亡是一种进化上保守且受到严格调控的细胞死亡途径。生理性细胞死亡对于通过持续清除不需要或多余的细胞来维持体内平衡和最佳生物学状态至关重要。仅含BH3结构域的促凋亡成员是细胞凋亡的强效诱导剂。仅含BH3结构域的促凋亡蛋白Noxa通过抑制抗凋亡Bcl-2家族蛋白Mcl-1以及其他导致Bax和Bak激活及线粒体膜通透性转换孔(MOMP)的蛋白成员来激活多种死亡途径。另一方面,在几种癌细胞系中,Puma由p53依赖性和p53非依赖性凋亡刺激诱导产生。此外,这种蛋白质参与多种生理和病理过程,如免疫、癌症和神经退行性疾病。未来的热休克研究可能会揭示热疗对Noxa和仅含BH3结构域蛋白的影响。这表明存在控制热休克细胞中Puma和Noxa mRNA翻译的转录后机制。这项研究也是概括针对半胱天冬酶所研究的不同反应机制的契机。