作者
Raúl Ramos,Kim T. Pham,Richard C. Prince,Leith B. Leiser-Miller,Maneeshi S. Prasad,Xiaojie Wang,Rachel C. Nordberg,Benjamin J. Bielajew,Jerry C. Hu,Kosuke Yamaga,Ji Won Oh,Tao Peng,Rupsa Datta,A. B. Astrowskaja,Axel A. Almet,Justin M. Burns,Yuchen Liu,Christian F. Guerrero‐Juarez,Bryant Q. Tran,Yi-Lin Chu,A. Nguyen,Tsai‐Ching Hsi,Norman T.‐L. Lim,Sandra Schöniger,Ruiqi Liu,Y.P. Pai,Chella Krishna Vadivel,Sandy Ingleby,Andrew E. McKechnie,Frank van Breukelen,Kyle L. Hoehn,John J. Rasweiler,Michinori Kohara,W. J. Loughry,Scott H. Weldy,Raymond Cosper,Chao‐Chun Yang,Sung‐Jan Lin,Kimberly L. Cooper,Sharlene E. Santana,Jeffrey E. Bradley,Michael A. Kiebish,Michelle A. Digman,David E. James,Amy E. Merrill,Qing Nie,Thomas F. Schilling,A. A. Astrowski,Eric O. Potma,Martín I. García‐Castro,Kyriacos A. Athanasiou,Richard R. Behringer,Maksim V. Plikus
摘要
Conventionally, the size, shape, and biomechanics of cartilages are determined by their voluminous extracellular matrix. By contrast, we found that multiple murine cartilages consist of lipid-filled cells called lipochondrocytes. Despite resembling adipocytes, lipochondrocytes were molecularly distinct and produced lipids exclusively through de novo lipogenesis. Consequently, lipochondrocytes grew uniform lipid droplets that resisted systemic lipid surges and did not enlarge upon obesity. Lipochondrocytes also lacked lipid mobilization factors, which enabled exceptional vacuole stability and protected cartilage from shrinking upon starvation. Lipid droplets modulated lipocartilage biomechanics by decreasing the tissue’s stiffness, strength, and resilience. Lipochondrocytes were found in multiple mammals, including humans, but not in nonmammalian tetrapods. Thus, analogous to bubble wrap, superstable lipid vacuoles confer skeletal tissue with cartilage-like properties without “packing foam–like” extracellular matrix.