Reply to “Bone morphogenetic protein's contribution to pulmonary artery hypertension”
نویسندگان
چکیده
We appreciate Dr. Epstein’s raising awareness of potential complications related to the usage of recombinant Bone Morphogenetic Protein (BMP).[5] Certainly, the list of potential adverse events are concerning to numerous audiences, including dentists, oral surgeons, orthopedists, and the biomedical science community.[6] However, in addition to the well‐documented complications such as marked dysphagia, acute upper airway inflammation, and respiratory distress, Dr Epstein raises the suspicion of a possible connection between BMP usage for spine fusion and the development of pulmonary arterial hypertension (PAH). We respectfully disagree with this point of view, and wish to highlight evidence that PAH likely develops from aberrant loss‐of‐function of the BMP pathway rather than over‐activation of the BMP pathway, as would be expected if recombinant BMP were to diffuse away from a local delivery site.
منابع مشابه
Commentary: Bone morphogenetic protein's contribution to pulmonary artery hypertension: Should this raise concern for patients undergoing spinal fusions with bone morphogenetic protein?
BACKGROUND Congenital pulmonary artery hypertension (PAH) has been clinically correlated in 70-80% of cases with mutations at the bone morphogenetic protein receptor 2 (BMPR2) genetic site. However, there is also clinical and basic science/laboratory literature indicating a dose-response relationship between BMP signaling and the evolution of PAH (e.g., increased endothelial, smooth muscle, and...
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BACKGROUND Mutations in the bmpr2 gene, encoding the type II bone morphogenetic protein (BMP) receptor, have been identified in patients with pulmonary arterial hypertension (PAH), implicating BMP signaling in PAH. The aim of this study was to assess BMP signaling and its physiological effects in a monocrotaline (MCT) model of PAH. METHODS AND RESULTS Expression of BMP receptors Ib and II, an...
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The bone morphogenetic protein (BMP) type II receptor (BMPR2) has a long cytoplasmic tail domain whose function is incompletely elucidated. Mutations in the tail domain of BMPR2 are found in familial cases of pulmonary arterial hypertension. To investigate the role of the tail domain of BMPR2 in BMP signaling, we generated a mouse carrying a Bmpr2 allele encoding a non-sense mediated decay-resi...
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Mutations in gene encoding for bone morphogenetic protein type 2 receptor (BMPR-2) have been reported in pulmonary arterial hypertension (PAH), but their functional relevance remains incompletely understood. BMP receptors expression was evaluated in human lungs and in cultured pulmonary artery smooth muscle cells (PASMCs) isolated from 19 idiopathic PAH patients and 9 heritable PAH patients wit...
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عنوان ژورنال:
دوره 7 شماره
صفحات -
تاریخ انتشار 2016