Hongjuan Wang - The First School of Clinical Medicine, Lanzhou University, Lanzhou ۷۳۰۰۰۰, Gansu, China
Lan Ma - Department of Plateau Medical Center, Qinghai University, Xining ۸۱۰۰۰۰, Qinghai, China
Qin Yu - The First School of Clinical Medicine, Lanzhou University, Lanzhou ۷۳۰۰۰۰, Gansu, China

Objective(s): Proliferation and migration of pulmonary artery smooth muscle cells (PASMCs) contribute to hypoxia-induced pulmonary hypertension (HPH). The transcription factor Cbp/p۳۰۰-interacting transactivator with Glu/Asp-rich carboxy-terminal domain ۲ (Cited۲) has been implicated in the control of tumor cells and mesenchymal stem cell (MSC) and cardiomyocyte growth or migration. Whether Cited۲ is involved in the proliferation and migration of PASMCs and the underlying mechanisms deserve to be explored. Materials and Methods: Cited۲ expression was detected in rat PASMCs under hypoxia conditions and HPH rat models. The effect of Cited۲ on the proliferation and migration of PASMC was detected by overexpression or knockdown of the Cited۲ gene. After PAMSCs were treated with recombinant TGF-β۱ and the lentivirus vector overexpressing Cited۲, expression of peroxisome proliferator-activated receptor gamma (PPARγ) was examined by western blotting.Results: We revealed that hypoxia down-regulated the expression of Cited۲ in PASMCs and rat pulmonary arteries. Cited۲ overexpression inhibited the proliferation and migration of PASMCs under hypoxia, while Cited۲ knockdown induced the proliferation and migration of PASMCs. Cited۲ inhibits the negative regulation of the TGF-β۱ pathway on PPARγ to inhibit the proliferation and migration of PASMCs.Conclusion: These findings suggest that increased Cited۲ expression contributes to the inhibition of PASMCs proliferation and migration by regulating TGF-β۱-mediated target gene expression in HPH and provides a new target for molecular therapy of HPH.

Cited۲, Hypoxia-induced pulmonary hypertension, Migration, Proliferation, Pulmonary artery smooth muscle cells