Departmental Papers (CBE)
Date of this Version
Cell differentiation in embryogenesis involves extensive changes in gene expression structural reorganization within the nucleus, including chromatin condensation and nucleoprotein immobilization. We hypothesized that nuclei in naive stem cells would therefore prove to be physically plastic and also more pliable than nuclei in differentiated cells. Micromanipulation methods indeed show that nuclei in human embryonic stem cells are highly deformable and stiffen 6-fold through terminal differentiation, and that nuclei in human adult stem cells possess an intermediate stiffness and deform irreversibly. Because the nucleo-skeletal component Lamin A/C is not expressed in either type of stem cell, we knocked down Lamin A/C in human epithelial cells and measured a deformability similar to that of adult hematopoietic stem cells. Rheologically, lamin-deficient states prove to be the most fluidlike, especially within the first ≈10 sec of deformation. Nuclear distortions that persist longer than this are irreversible, and fluorescence- imaged microdeformation with photobleaching confirms that chromatin indeed flows, distends, and reorganizes while the lamina stretches. The rheological character of the nucleus is thus set largely by nucleoplasm/chromatin, whereas the extent of deformation is modulated by the lamina.
chromatin remodeling, cell mechanics, nuclear plasticity
Pajerowski, J. D., Dahl, K., Zhong, F. L., Sammak, P. J., & Discher, D. E. (2007). Physical plasticity of the nucleus in stem cell differentiation. Retrieved from https://repository.upenn.edu/cbe_papers/115
Date Posted: 10 April 2008
This document has been peer reviewed.
Copyright National Academy of Sciences. Reprinted from Proceedings of the National Academy of Sciences, Volume 104, Issue 40, October 2007, pages 15619–15624. Publisher URL: www.pnas.org/cgi/doi/10.1073/pnas.0702576104