Adult neural stem cells have latent inflammatory potential that is kept suppressed by <i>Tcf4</i> to facilitate adult neurogenesis.

Abstract

Inflammation is known to adversely affect adult neurogenesis, wherein the source of inflammation is largely thought to be extraneous to the neurogenic niche. Here, we demonstrate that the adult hippocampal neural progenitors harbor an inflammatory potential that is proactively suppressed by transcription factor 4 (<i>Tcf4</i>). Deletion of <i>Tcf4</i> in hippocampal <i>nestin</i>-expressing progenitors causes loss of proliferative capacity and acquisition of myeloid inflammatory properties. This transformation abolishes their differentiation potential and causes production of detrimental factors that adversely affect niche cells, causing inflammation in the dentate gyrus. Thus, on one hand, <i>Tcf4</i> deletion causes abrogation of proliferative progenitors leading to reduction of adult neurogenesis, while on the other, their accompanying inflammatory transformation inflicts inflammation in the niche. Taken together, we provide the first evidence for a latent inflammatory potential of adult hippocampal neural progenitors and identify <i>Tcf4</i> as a critical regulator that facilitates adult neurogenesis via proactive suppression of this detrimental potential.