Narbonne Patrick, Maddox Paul S, Labbé Jean-Claude
Department of Pathology and Cell Biology, Institut de Recherche en Immunologie et en Cancérologie (IRIC), Université de Montréal, Montréal, Québec, Canada.
Department of Biology, University of North Carolina Chapel Hill, Chapel Hill, NC, United States of America.
PLoS Genet. 2017 Apr 14;13(4):e1006738. doi: 10.1371/journal.pgen.1006738. eCollection 2017 Apr.
Under replete growth conditions, abundant nutrient uptake leads to the systemic activation of insulin/IGF-1 signalling (IIS) and the promotion of stem cell growth/proliferation. Activated IIS can stimulate the ERK/MAPK pathway, the activation of which also supports optimal stem cell proliferation in various systems. Stem cell proliferation rates can further be locally refined to meet the resident tissue's need for differentiated progeny. We have recently shown that the accumulation of mature oocytes in the C. elegans germ line, through DAF-18/PTEN, inhibits adult germline stem cell (GSC) proliferation, despite high systemic IIS activation. We show here that this feedback occurs through a novel cryptic signalling pathway that requires PAR-4/LKB1, AAK-1/AMPK and PAR-5/14-3-3 to inhibit the activity of MPK-1/MAPK, antagonize IIS, and inhibit both GSC proliferation and the production of additional oocytes. Interestingly, our results imply that DAF-18/PTEN, through PAR-4/LKB1, can activate AAK-1/AMPK in the absence of apparent energy stress. As all components are conserved, similar signalling cascades may regulate stem cell activities in other organisms and be widely implicated in cancer.
在充足的生长条件下,丰富的营养物质摄取会导致胰岛素/胰岛素样生长因子-1信号通路(IIS)的全身激活,并促进干细胞生长/增殖。激活的IIS可以刺激ERK/MAPK通路,该通路的激活也支持各种系统中最佳的干细胞增殖。干细胞增殖率可以进一步在局部进行微调,以满足驻留组织对分化后代的需求。我们最近发现,尽管全身IIS高度激活,但秀丽隐杆线虫生殖系中成熟卵母细胞通过DAF-18/PTEN的积累会抑制成年生殖系干细胞(GSC)的增殖。我们在此表明,这种反馈通过一条新的隐秘信号通路发生,该通路需要PAR-4/LKB1、AAK-1/AMPK和PAR-5/14-3-3来抑制MPK-1/MAPK的活性,拮抗IIS,并抑制GSC增殖和额外卵母细胞的产生。有趣的是,我们的结果表明,DAF-18/PTEN可以通过PAR-4/LKB1在没有明显能量应激的情况下激活AAK-1/AMPK。由于所有成分都是保守的,类似的信号级联可能在其他生物体中调节干细胞活动,并广泛涉及癌症。