Lipolysis of bone marrow adipocytes is required to fuel bone and the marrow niche during energy deficits.
Ziru LiEmily BowersJunxiong ZhuHui YuJulie HardijDevika P BagchiHiroyuki MoriKenneth T LewisKatrina GrangerRebecca L SchillSteven M RomanelliSimin AbrishamiKurt D HankensonKanakadurga SingerClifford J RosenOrmond A MacDougaldPublished in: eLife (2022)
To investigate roles for bone marrow adipocyte (BMAd) lipolysis in bone homeostasis, we created a BMAd-specific Cre mouse model in which we knocked out adipose triglyceride lipase (ATGL, Pnpla2 gene). BMAd- Pnpla2 -/- mice have impaired BMAd lipolysis, and increased size and number of BMAds at baseline. Although energy from BMAd lipid stores is largely dispensable when mice are fed ad libitum, BMAd lipolysis is necessary to maintain myelopoiesis and bone mass under caloric restriction. BMAd-specific Pnpla2 deficiency compounds the effects of caloric restriction on loss of trabecular bone in male mice, likely due to impaired osteoblast expression of collagen genes and reduced osteoid synthesis. RNA sequencing analysis of bone marrow adipose tissue reveals that caloric restriction induces dramatic elevations in extracellular matrix organization and skeletal development genes, and energy from BMAd is required for these adaptations. BMAd-derived energy supply is also required for bone regeneration upon injury, and maintenance of bone mass with cold exposure.
Keyphrases
- adipose tissue
- bone regeneration
- bone marrow
- bone mineral density
- insulin resistance
- extracellular matrix
- high fat diet
- mesenchymal stem cells
- soft tissue
- mouse model
- bone loss
- high fat diet induced
- traumatic brain injury
- type diabetes
- genome wide identification
- high intensity
- skeletal muscle
- transcription factor
- wild type