Multiple phases of chondrocyte enlargement underlie differences in skeletal proportions

Nature. 2013 Mar 21;495(7441):375-8. doi: 10.1038/nature11940. Epub 2013 Mar 13.


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. However, the mechanisms of chondrocyte volume enlargement have remained a mystery. Here we use quantitative phase microscopy 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, 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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Bone and Bones / cytology*
  • Cell Size
  • Cells, Cultured
  • Chondrocytes / cytology*
  • Growth Plate / cytology*
  • Growth Plate / growth & development*
  • Insulin-Like Growth Factor I / metabolism
  • Metatarsal Bones / cytology
  • Mice
  • Tibia / cytology


  • insulin-like growth factor-1, mouse
  • Insulin-Like Growth Factor I