通过AP-3复杂依赖调节死亡途径死亡的细胞在氨基酸缺乏条件下支持生存的细胞
Svyatoslav S Sokolov1, Ekaterina A Smirnova2, Natalia A Kireeva2
1Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119991, Russia. sviatoslav.sokolov@gmail.com.
Biochemistry. Biokhimiia
|August 31, 2025
概括
将酵母细胞加热到52°C就会触发一个被编程的死亡途径,释放营养物质,在氨基酸饥饿期间支持生存细胞. 这一过程依赖于 lysosomal 膜分解,帮助缺乏营养的酵母种群.
科学领域:
- 细胞生物学
- 微生物学
- 生物化学
背景情况:
- 单细胞生物可以在饥饿期间经历编程细胞死亡,以支持幸存的种群.
- 将Saccharomyces cerevisiae酵母细胞加热到51°C会诱导特定的细胞死亡途径,包括溶解体和血分解.
研究的目的:
- 研究热引起的细胞死亡对饥饿酵母提供营养的作用.
- 确定 lysosomal 膜分解途径是否对于释放促进生长的物质至关重要.
主要方法:
- 酵母细胞处理:在52°C加热,沸,使用缺乏AP-3复合物的突变物.
- 在氨基酸缺乏的情况下评估活酵母细胞的生长刺激.
- 细胞介质的光谱和质谱分析.
主要成果:
- 被加热到52°C时死亡的酵母细胞在氨基酸缺乏下显著刺激了活细胞的生长.
- 缺乏AP-3复合体的突变细胞无法降解解酶体膜,因此无法支持生长.
- 从52°C加热的细胞中含有吸收短波长的物质,暗示核酸水解产物.
结论:
- 在酵母中因热引起的细胞死亡,特别是通过 lysosomal 膜水解,释放的化合物在饥饿期间支持生存细胞.
- 对于这种营养共享机制来说,AP-3复合体至关重要.
- 核酸水解产物可能是促进活存酵母细胞生长的原因.
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