Hematopoietic cell‐intrinsic Wnt4 promotes stem cell expansion and self‐renewal. Wnt4‐deficient (Wnt4Δ/Δ) stem cells display decreased lymphoid potential, increased mitochondrial superoxide and stress‐associated JNK activity, and cell cycle perturbations, including increased p16INK4a expression. Wnt4 thus favors stem cell maintenance, particularly in a situation of bone marrow recovery, and reduces the release of proinflammatory cytokines in the bone marrow environment.
Abstract
Although intracellular Wnt signaling pathways need to be tightly regulated to promote hematopoietic stem cell self‐renewal, the source and identity of important Wnt ligands in the bone marrow is still largely unknown. The noncanonical ligand Wnt4 is expressed in the bone marrow as well as in the stroma, and its overexpression in fetal liver cells facilitates thymic recovery; however, its impact on adult hematopoietic stem cell function remains unclear. Here, we report that the deletion of Wnt4 from hematopoietic cells in mice (Wnt4 Δ/Δ) resulted in decreased lymphopoiesis at steady state. This was likely at least in part due to the increased proinflammatory environment present in the bone marrow of Wnt4 Δ/Δ mice. Wnt4 Δ/Δ hematopoietic stem cells displayed reduced reconstitution capacity in serial transplants, thus demonstrating defective self‐renewal, and they expanded poorly in response to lipopolysaccharide stimulation. This appeared to be the result of the absence of Wnt4 in stem/progenitor cells, as myeloid‐restricted Wnt4 deletion had no notable effect. Finally, we observed that Wnt4 Δ/Δ stem/progenitor cells were more quiescent, presenting enhanced levels of stress‐associated JNK phosphorylation and p16INK4a expression, likely contributing to the reduced expansion observed in transplants. In conclusion, our results identify a new, largely autocrine role for Wnt4 in hematopoietic stem cell self‐renewal, suggesting that regulation of Wnt signaling in hematopoiesis may not need Wnt secretion and could be independent of morphogen gradients.