| Literature DB >> 29775577 |
Yahav Yosefzon1, Despina Soteriou1, Alona Feldman1, Lana Kostic1, Elle Koren1, Samara Brown2, Roi Ankawa1, Egor Sedov1, Fabian Glaser3, Yaron Fuchs4.
Abstract
Apoptosis culminates in the activation of caspase-3, which plays an important role in implementing the cell death program. Here, we reveal a non-apoptotic role of caspase-3 as a key regulator of cell proliferation and organ size. Caspase-3 is specifically activated in the proliferating cells of the sebaceous gland, but does not instruct cell elimination. Deletion or chemical inhibition of caspase-3 diminishes cell proliferation, decreases cell number and reduces sebaceous gland size in vivo. Exploring the underlying mechanism, we demonstrate that α-catenin is cleaved by caspase-3, thus facilitating the activation and nuclear translocation of yes-associated protein (YAP), a vital regulator of organ size. Accordingly, activation of caspase-3 leads to YAP-dependent organ size augmentation. Finally, we show that X-linked inhibitor of apoptosis protein (XIAP) serves as an endogenous feedback antagonist for the caspase-3/YAP signaling module. Taken together, we report here a molecular mechanism wherein the apoptotic machinery is refocused to regulate cell proliferation and orchestrate organ size.Entities:
Keywords: XIAP; YAP; apoptosis; caspase; catenin; hair follicle; organ size; proliferation; sebaceous gland; skin
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Year: 2018 PMID: 29775577 DOI: 10.1016/j.molcel.2018.04.019
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970