Microglia-derived TNF alpha induces apoptosis in neural precursor cells via transcriptional activation of the Bcl-2 family member Puma

作者：Guadagno J; Xu X; Karajgikar M; Brown A; Cregan S P^*

来源：Cell Death & Disease, 2013, 4(3): e538.

DOI：10.1038/cddis.2013.59

• apoptosis
• neuroinflammation
• neural precursor cells
• microglia

Neuroinflammation is a common feature of acute neurological conditions such as stroke and spinal cord injury, as well as neurodegenerative conditions such as Parkinson's disease, Alzheimer's disease, and amyotrophic lateral sclerosis. Previous studies have demonstrated that acute neuroinflammation can adversely affect the survival of neural precursor cells (NPCs) and thereby limit the capacity for regeneration and repair. However, the mechanisms by which neuroinflammatory processes induce NPC death remain unclear. Microglia are key mediators of neuroinflammation and when activated to induce a pro-inflammatory state produce a number of factors that could affect NPC survival. Importantly, in the present study we demonstrate that tumor necrosis factor alpha (TNF alpha) produced by lipopolysaccharide-activated microglia is necessary and sufficient to trigger apoptosis in mouse NPCs in vitro. Furthermore, we demonstrate that microglia-derived TNF alpha induces NPC apoptosis via a mitochondrial pathway regulated by the Bcl-2 family protein Bax. BH3-only proteins are known to play a key role in regulating Bax activation and we demonstrate that microglia-derived TNF alpha induces the expression of the BH3-only family member Puma in NPCs via an NF-kappa B-dependent mechanism. Specifically, we show that NF-kappa B is activated in NPCs treated with conditioned media from activated microglia and that Puma induction and NPC apoptosis is blocked by the NF-kappa B inhibitor BAY-117082. Importantly, we have determined that NPC apoptosis induced by activated microglia-derived TNF alpha is attenuated in Puma-deficient NPCs, indicating that Puma induction is required for NPC death. Consistent with this, we demonstrate that Puma-deficient NPCs exhibit an similar to 13-fold increase in survival as compared with wild-type NPCs following transplantation into the inflammatory environment of the injured spinal cord in vivo. In summary, we have identified a key signaling pathway that regulates neuroinflammation induced apoptosis in NPCs in vitro and in vivo that could be targeted to promote regeneration and repair in diverse neurological conditions. Cell Death and Disease (2013) 4, e538; doi:10.1038/cddis.2013.59; published online 14 March 2013

• 出版日期2013-3