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Mol Ther. 2017 Aug 2;25(8):1974-1987. doi: 10.1016/j.ymthe.2017.01.008. Epub 2017 Jul 15.

Strategic Targeting of Multiple BMP Receptors Prevents Trauma-Induced Heterotopic Ossification.

Author information

1
Department of Surgery, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
2
Stanford University, Palo Alto, CA 94305, USA.
3
Acceleron Pharma, Cambridge, MA 02139, USA.
4
Department of Surgery, Massachusetts General Hospital, Boston, MA 02114, USA.
5
Hagey Research Laboratory, Department of Surgery, Stanford University, Palo Alto, CA 94305, USA.
6
Regenerative Medicine Department, Naval Medical Research Center, Silver Spring, MD 20910, USA.
7
Department of Medicine, Harvard University, Boston, MA 02115, USA.
8
Department of Biological and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, MI 48109, USA.
9
Department of Surgery, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: blevi@umich.edu.

Abstract

Trauma-induced heterotopic ossification (tHO) is a condition of pathologic wound healing, defined by the progressive formation of ectopic bone in soft tissue following severe burns or trauma. Because previous studies have shown that genetic variants of HO, such as fibrodysplasia ossificans progressiva (FOP), are caused by hyperactivating mutations of the type I bone morphogenetic protein receptor (T1-BMPR) ACVR1/ALK2, studies evaluating therapies for HO have been directed primarily toward drugs for this specific receptor. However, patients with tHO do not carry known T1-BMPR mutations. Here we show that, although BMP signaling is required for tHO, no single T1-BMPR (ACVR1/ALK2, BMPR1a/ALK3, or BMPR1b/ALK6) alone is necessary for this disease, suggesting that these receptors have functional redundancy in the setting of tHO. By utilizing two different classes of BMP signaling inhibitors, we developed a translational approach to treatment, integrating treatment choice with existing diagnostic options. Our treatment paradigm balances either immediate therapy with reduced risk for adverse effects (Alk3-Fc) or delayed therapy with improved patient selection but greater risk for adverse effects (LDN-212854).

KEYWORDS:

BMP receptors; BMP signaling; stem cells

PMID:
28716575
PMCID:
PMC5542633
DOI:
10.1016/j.ymthe.2017.01.008
[Indexed for MEDLINE]
Free PMC Article

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