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The peroxisome proliferator‐activated receptor gamma (PPARγ) controls adipogenesis and metabolism. We demonstrate here that the absence of PPARγ in fat has potent osteogenic activities, which affect haematopoiesis. The congenital absence of PPARγ in fat of lipodystrophic PPARγhyp/hyp mice, strongly enhanced bone mass and consequentially reduced the bone‐marrow cavity. Consistent with this, PPARγhyp/hyp mice had a significant decrease in bone marrow cellularity and resorted to extramedullary haematopoiesis in the spleen to maintain haematopoiesis. Our data indicate that antagonizing PPARγ activity in fat could be an effective way to combat osteoporosis and suggest that haematopoietic function should be scrutinized in lipodystrophic subjects.
Lipodystrophy, Bone and Bones, Spine, Mice, Inbred C57BL, PPAR gamma, Mice, Hematopoiesis, Extramedullary, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Animals, RNA, Messenger, Spleen
Lipodystrophy, Bone and Bones, Spine, Mice, Inbred C57BL, PPAR gamma, Mice, Hematopoiesis, Extramedullary, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Animals, RNA, Messenger, Spleen
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 112 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |