Transcriptional regulation of cyclophilin D by BMP/Smad signaling and its role in osteogenic differentiation

被引:17
作者
Sautchuk, Rubens [1 ]
Kalicharan, Brianna H. [1 ]
Escalera-Rivera, Katherine [1 ]
Jonason, Jennifer H. [1 ,2 ]
Porter, George A. [3 ]
Awad, Hani A. [1 ,4 ]
Eliseev, Roman A. [1 ,2 ,5 ]
机构
[1] Univ Rochester, Ctr Musculoskeletal Res, Rochester, NY 14627 USA
[2] Univ Rochester, Dept Pathol, Rochester, NY 14627 USA
[3] Univ Rochester, Dept Pediat, Div Cardiol, Rochester, NY USA
[4] Univ Rochester, Dept Biomed Engn, Rochester, NY USA
[5] Univ Rochester, Dept Pharmacol & Physiol, Rochester, NY 14627 USA
关键词
cyclophilin D; mitochondria; permeability transition; BMP; Smad; osteoprogenitor; bone; Human; Mouse; MITOCHONDRIAL PERMEABILITY TRANSITION; MYOGENIC DIFFERENTIATION; SUPEROXIDE-PRODUCTION; ATP SYNTHASE; CELL-DEATH; PORE; INHIBITION; CHANNEL; MECHANISMS; MATURATION;
D O I
10.7554/eLife.75023
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cyclophilin D (CypD) promotes opening of the mitochondrial permeability transition pore (MPTP) which plays a key role in both cell physiology and pathology. It is, therefore, beneficial for cells to tightly regulate CypD and MPTP but little is known about such regulation. We have reported before that CypD is downregulated and MPTP deactivated during differentiation in various tissues. Herein, we identify BMP/Smad signaling, a major driver of differentiation, as a transcriptional regulator of the CypD gene, Ppif. Using osteogenic induction of mesenchymal lineage cells as a BMP/Smad activation-dependent differentiation model, we show that CypD is in fact transcriptionally repressed during this process. The importance of such CypD downregulation is evidenced by the negative effect of CypD 'rescue' via gain-of-function on osteogenesis both in vitro and in a mouse model. In sum, we characterized BMP/Smad signaling as a regulator of CypD expression and elucidated the role of CypD downregulation during cell differentiation.
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页数:29
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