POT1a deficiency in mesenchymal niches perturbs B-lymphopoiesis

Protection of telomeres 1a (POT1a) is a telomere binding protein. A decrease of POT1a is related to myeloid-skewed haematopoiesis with ageing, suggesting that protection of telomeres is essential to sustain multi-potency. Since mesenchymal stem cells (MSCs) are a constituent of the hematopoietic niche in bone marrow, their dysfunction is associated with haematopoietic failure. However, the importance of telomere protection in MSCs has yet to be elucidated. Here, we show that genetic deletion of POT1a in MSCs leads to intracellular accumulation of fatty acids and excessive ROS and DNA damage, resulting in impaired osteogenic-differentiation. Furthermore, MSC-specific POT1a deficient mice exhibited skeletal retardation due to reduction of IL-7 producing bone lining osteoblasts. Single-cell gene expression profiling of bone marrow from POT1a deficient mice revealed that B-lymphopoiesis was selectively impaired. These results demonstrate that bone marrow microenvironments composed of POT1a deficient MSCs fail to support B-lymphopoiesis, which may underpin age-related myeloid-bias in haematopoiesis. POT1a is crucial for osteogenic-differentiation from mesenchymal stem cells (MSCs), and the ability to support B-lymphopoiesis is diminished in bone marrow microenvironments with POT1a deletion in MSCs

Automated summary

Protection of telomeres 1a (POT1a) is crucial for maintaining the stability of the bone marrow microenvironment and supporting B-lymphopoiesis. Deletion of POT1a in mesenchymal stem cells (MSCs) may lead to bone marrow dysfunction and myeloid skewing.