Guedes Joana P, Baptista Vitória, Santos-Pereira Cátia, Sousa Maria João, Manon Stéphen, Chaves Susana R, Côrte-Real Manuela
Centre of Molecular and Environmental Biology (CBMA), Department of Biology, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.
Centro de Investigacíon Médica Aplicada (CIMA), Universidad de Navarra, 31008, Pamplona, Spain.
Apoptosis. 2022 Jun;27(5-6):368-381. doi: 10.1007/s10495-022-01717-0. Epub 2022 Apr 1.
Proteins of the Bcl-2 protein family, including pro-apoptotic Bax and anti-apoptotic Bcl-xL, are critical for mitochondrial-mediated apoptosis regulation. Since yeast lacks obvious orthologs of Bcl-2 family members, heterologous expression of these proteins has been used to investigate their molecular and functional aspects. Active Bax is involved in the formation of mitochondrial outer membrane pores, through which cytochrome c (cyt c) is released, triggering a cascade of downstream apoptotic events. However, when in its inactive form, Bax is largely cytosolic or weakly bound to mitochondria. Given the central role of Bax in apoptosis, studies aiming to understand its regulation are of paramount importance towards its exploitation as a therapeutic target. So far, studies taking advantage of heterologous expression of human Bax in yeast to unveil regulation of Bax activation have relied on the use of artificial mutated or mitochondrial tagged Bax for its activation, rather than the wild type Bax (Bax α). Here, we found that cell death could be triggered in yeast cells heterologoulsy expressing Bax α with concentrations of acetic acid that are not lethal to wild type cells. This was associated with Bax mitochondrial translocation and cyt c release, closely resembling the natural Bax function in the cellular context. This regulated cell death process was reverted by co-expression with Bcl-xL, but not with Bcl-xLΔC, and in the absence of Rim11p, the yeast ortholog of mammalian GSK3β. This novel system mimics human Bax α regulation by GSK3β and can therefore be used as a platform to uncover novel Bax regulators and explore its therapeutic modulation.
Bcl-2蛋白家族的蛋白质,包括促凋亡的Bax和抗凋亡的Bcl-xL,对于线粒体介导的细胞凋亡调节至关重要。由于酵母缺乏Bcl-2家族成员明显的直系同源物,因此这些蛋白质的异源表达已被用于研究它们的分子和功能方面。活性Bax参与线粒体外膜孔的形成,细胞色素c(cyt c)通过该孔释放,从而触发一系列下游凋亡事件。然而,当处于非活性形式时,Bax主要位于细胞质中或与线粒体弱结合。鉴于Bax在细胞凋亡中的核心作用,旨在了解其调节机制的研究对于将其开发为治疗靶点至关重要。到目前为止,利用人Bax在酵母中的异源表达来揭示Bax激活调节的研究依赖于使用人工突变或线粒体标记的Bax来激活它,而不是野生型Bax(Baxα)。在这里,我们发现,用对野生型细胞无致死性的乙酸浓度可以触发异源表达Baxα的酵母细胞死亡。这与Bax向线粒体的转位和cyt c的释放有关,与细胞环境中Bax的天然功能非常相似。这种受调节的细胞死亡过程通过与Bcl-xL共表达而逆转,但与Bcl-xLΔC共表达则不能逆转,并且在没有Rim11p(哺乳动物GSK3β的酵母直系同源物)的情况下也不能逆转。这个新系统模拟了GSK3β对人Baxα的调节,因此可以用作揭示新型Bax调节剂和探索其治疗调节作用的平台。