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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Msx2 is required for vascular smooth muscle cells osteoblastic differentiation but not calcification in insulin-resistant ob/ob mice

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Author(s):
Andrade, Maria Claudina ; Carmo, Luciana S. ; Farias-Silva, Elisangela ; Liberman, Marcel
Total Authors: 4
Document type: Journal article
Source: ATHEROSCLEROSIS; v. 265, p. 14-21, OCT 2017.
Web of Science Citations: 5
Abstract

Background and aims: Obesity and diabetes potentiate vascular calcification by increasing vascular smooth muscle cells osteoblastic differentiation mediated by the transcription factor Msx2 and bone morphogenetic protein-2 signaling. However, Bmp-2/Msx2 crosstalk to induce VSMC osteogenic phenotype transition and calcification is poorly understood in diabetes. We aimed to investigate mechanisms underlying Bmp-2-driven VSMC osteogenic differentiation and calcification in leptindeficient ob/ob mice. Methods: We incubated VSMC from ob/ob mice and wild type C57BL/6 littermates with or without Bmp2. We used loss-of-function experiments to investigate the role of Msx2 in Bmp-2-induced ob/ob VSMC osteochondrogenic differentiation and calcification by transfecting Msx2 siRNA into VSMC. Results: Baseline ob/ob VSMC and aorta showed increased Msx2, Runx2, alkaline phosphatase mRNA and protein expression, which further increased in Bmp-2-incubated ob/ob VSMC, therefore augmenting ob/ob VSMC calcification in comparison to wild type VSMC. Accordingly, signaling pathways to induce VSMC osteogenic differentiation, such as Smad1/5 phosphorylation increased in ob/ob versus wild type aorta. In comparison to wild type VSMC, Msx2 siRNA transfected VSMC decreased Bmp-2-dependent osteochondrogenic differentiation response by abrogating Msx2, Runx2, Alpl expression in ob/ob but not in wild type VSMC. Nonetheless, Msx2 inhibition did not decrease calcification in Bmp-2 stimulated ob/ob VSMC in vitro. Conclusions: Our data support a crucial role of Msx2 for ob/ob VSMC osteochondrogenic differentiation, however, Msx2 signaling alone is not sufficient for ob/ob VSMC calcification after Bmp-2 stimulation in vitro. These findings can be translated into novel perspectives for the understanding of the mechanisms and to provide therapeutic targets underlying vascular calcification in type 2 diabetes. (C) 2017 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 13/09652-0 - Mechanisms of excentric remodeling associated with vascular calcification in obesity and insulin resistance
Grantee:Luciana Simao Do Carmo
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 13/09611-2 - Mechanisms of excentric remodeling associated with vascular calcification in obesity and insulin resistance
Grantee:Marcel Liberman
Support Opportunities: Regular Research Grants
FAPESP's process: 10/07455-5 - Impact of insulin resistance on the progression of vascular calcification
Grantee:Marcel Liberman
Support Opportunities: Regular Research Grants