| Literature DB >> 26140478 |
Buer Sen1, Zhihui Xie1, Gunes Uzer1, William R Thompson2, Maya Styner1, Xin Wu1, Janet Rubin1.
Abstract
Depolymerization of the actin cytoskeleton induces nuclear trafficking of regulatory proteins and global effects on gene transcription. We here show that in mesenchymal stem cells (MSCs), cytochalasin D treatment causes rapid cofilin-/importin-9-dependent transfer of G-actin into the nucleus. The continued presence of intranuclear actin, which forms rod-like structures that stain with phalloidin, is associated with induction of robust expression of the osteogenic genes osterix and osteocalcin in a Runx2-dependent manner, and leads to acquisition of osteogenic phenotype. Adipogenic differentiation also occurs, but to a lesser degree. Intranuclear actin leads to nuclear export of Yes-associated protein (YAP); maintenance of nuclear YAP inhibits Runx2 initiation of osteogenesis. Injection of cytochalasin into the tibial marrow space of live mice results in abundant bone formation within the space of 1 week. In sum, increased intranuclear actin forces MSC into osteogenic lineage through controlling Runx2 activity; this process may be useful for clinical objectives of forming bone.Entities:
Keywords: Bone; Cofilin; Cytoskeleton; Importin 9; Mesenchymal stem cells; Runx2; Yes-associated protein
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Year: 2015 PMID: 26140478 PMCID: PMC4788101 DOI: 10.1002/stem.2090
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277