Multiple phases of chondrocyte enlargement underlie differences in skeletal proportions

被引:293
作者
Cooper, Kimberly L. [1 ]
Oh, Seungeun [2 ]
Sung, Yongjin [3 ]
Dasari, Ramachandra R. [3 ]
Kirschner, Marc W. [2 ]
Tabin, Clifford J. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[3] MIT, George R Harrison Spect Lab, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
LONGITUDINAL BONE-GROWTH; PLATE CHONDROCYTES; VOLUME INCREASE; FACTOR-I; HYPERTROPHY; PERFORMANCE; MECHANISMS; HINDLIMB; RATS; AGE;
D O I
10.1038/nature11940
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The wide diversity of skeletal proportions in mammals is evident upon a survey of any natural history museum's collections and allows us to distinguish between species even when reduced to their calcified components. Similarly, each individual is comprised of a variety of bones of differing lengths. The largest contribution to the lengthening of a skeletal element, and to the differential elongation of elements, comes from a dramatic increase in the volume of hypertrophic chondrocytes in the growth plate as they undergo terminal differentiation(1-7). However, the mechanisms of chondrocyte volume enlargement have remained a mystery(8-11). Here we use quantitative phase microscopy(12) to show that mammalian chondrocytes undergo three distinct phases of volume increase, including a phase of massive cell swelling in which the cellular dry mass is significantly diluted. In light of the tight fluid regulatory mechanisms known to control volume in many cell types(13), this is a remarkable mechanism for increasing cell size and. regulating growth rate. It is, however, the duration of the final phase of volume enlargement by proportional dry mass increase at low density that varies most between rapidly and slowly elongating growth plates. Moreover, we find that this third phase is locally regulated through a mechanism dependent on insulin-like growth factor. This study provides a framework for understanding how skeletal size is regulated and for exploring how cells sense, modify and establish a volume set point.
引用
收藏
页码:375 / 378
页数:4
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