Mechanical force-driven TNF? endocytosis governs stem cell homeostasis.

ABSTRACT: Mesenchymal stem cells (MSCs) closely interact with the immune system, and they are known to secrete inflammatory cytokines in response to stress stimuli. The biological function of MSC-derived inflammatory cytokines remains elusive. Here, we reveal that even under physiological conditions, MSCs produce and release a low level of tumor necrosis factor alpha (TNF?), which is unexpectedly required for preserving the self-renewal and differentiation of MSCs via autocrine/paracrine signaling. Furthermore, TNF? critically maintains MSC function in vivo during bone homeostasis. Mechanistically, we unexpectedly discovered that physiological levels of TNF? safeguard MSC homeostasis in a receptor-independent manner through mechanical force-driven endocytosis and that endocytosed TNF? binds to mammalian target of rapamycin (mTOR) complex 2 and restricts mTOR signaling. Importantly, inhibition of mTOR signaling by rapamycin serves as an effective osteoanabolic therapeutic strategy to protect against TNF? deficiency and mechanical unloading. Collectively, these findings unravel the physiological framework of the dynamic TNF? shuttle-based mTOR equilibrium that governs MSC and bone homeostasis.

SUBMITTER: Yu W 

PROVIDER: S-EPMC7775432 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature