| First Author | Guo M | Year | 2015 |
| Journal | Mol Cell Biol | Volume | 35 |
| Issue | 12 | Pages | 2119-30 |
| PubMed ID | 25870110 | Mgi Jnum | J:224102 |
| Mgi Id | MGI:5661271 | Doi | 10.1128/MCB.01414-14 |
| Citation | Guo M, et al. (2015) Novel role for cyclophilin A in regulation of chondrogenic commitment and endochondral ossification. Mol Cell Biol 35(12):2119-30 |
| abstractText | Recent studies showed that cyclophilin A (CypA) promotes NF-kappaB/p65 nuclear translocation, resulting in enhanced NF-kappaB activity and altered expression of its target genes, such as the Sox9 transcriptional factor, which plays a critical role in chondrogenic differentiation and endochondral ossification. In this report, we unveil the role of CypA in signal-induced chondrogenic differentiation and endochondral ossification. Expression levels of the chondrogenic differentiation markers and transcriptional regulators Sox9 and Runx2 were all significantly lower in CypA knockdown chondrogenic cells than in wild-type cells, indicating that CypA plays a functional role in chondrogenic differentiation. In vitro differentiation studies using micromass cultures of mouse limb bud cells further supported the conclusion that CypA is needed for chondrogenic differentiation. Newborn CypA-deficient pups double stained with alcian blue and alizarin red exhibited generalized, pronounced skeletal defects, while high-resolution micro-computed tomography (microCT) analyses of the femurs and lumbar vertebrae revealed delayed or incomplete endochondral ossification. Comparative histology and immunohistochemistry (IHC) analyses further verified the effects of CypA deficiency on chondrogenic differentiation. Our results provide evidence for the important contribution of CypA as a pertinent component acting through NF-kappaB-Sox9 in regulation of chondrogenesis signaling. These findings are important to better understand signal-induced chondrogenesis of chondrogenic progenitors in physiological and pathophysiological contexts. |
