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

Author:

Sautchuk Rubens1ORCID,Kalicharan Brianna H1,Escalera-Rivera Katherine1,Jonason Jennifer H12,Porter George A3,Awad Hani A14ORCID,Eliseev Roman A125ORCID

Affiliation:

1. Center for Musculoskeletal Research, University of Rochester

2. Department of Pathology, University of Rochester

3. Department of Pediatrics, Division of Cardiology, University of Rochester

4. Department of Biomedical Engineering, University of Rochester

5. Department of Pharmacology & Physiology, University of Rochester

Abstract

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.

Funder

National Institute of Dental and Craniofacial Research

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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