Both transforming growth factor beta (TGF-beta) and latent TGF-beta binding protein (LTBP) play important roles in the development of the embryonic heart as proper signaling through the TGF-beta pathway is needed both for regulating cell proliferation and gene expression. However, cells secrete TGF-beta in a latent form bound to the LTBP as large latent complex (LLC). The release of TGF-beta from this complex is regulated by the activity of proteases. Our proposal consists of generating transgenic mice that express truncated form of TGF-beta binding region (CR3) of LTBP-1 under two heart specific promoters, for alpha-myelin heavy chain ands myelin light chain (alpha-MHC, MLC). In that way we will try to characterize the consequences of inappropriate activation of latent TGF-beta, as a result of disruption of its binding to LTBP, without affecting the expression of TGF-beta and LTBP. We will test the hypothesis that expression of CR3 will result in increased levels of active TGF-beta in the heart and it's consequences on heart development. We will monitor active TGF-beta in heart during prenatal and postnatal development. As a control of our hypothesis, experiments designed to counter the actions of excess TGF-beta in the heart will be performed. Those experiments will include incubation with TGF-beta neutralizing antibodies and LAP peptides. This should revert the phenotype toward the wild type situation. These experiments will enhance our understanding of TGF-beta function in early and late development of the mouse heart. We anticipate that these results will contribute to our understanding of the extra-cellular control of signaling molecules such as TGF-beta and the role of LTBP in that signaling.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HL067542-01
Application #
6339774
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Program Officer
Commarato, Michael
Project Start
2001-09-13
Project End
Budget Start
2001-09-13
Budget End
2002-09-12
Support Year
1
Fiscal Year
2001
Total Cost
$34,832
Indirect Cost
Name
New York University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
Yoshinaga, Keiji; Obata, Hiroto; Jurukovski, Vladimir et al. (2008) Perturbation of transforming growth factor (TGF)-beta1 association with latent TGF-beta binding protein yields inflammation and tumors. Proc Natl Acad Sci U S A 105:18758-63
Colarossi, Cristina; Chen, Yan; Obata, Hiroto et al. (2005) Lung alveolar septation defects in Ltbp-3-null mice. Am J Pathol 167:419-28
Mazzieri, Roberta; Jurukovski, Vladimir; Obata, Hiroto et al. (2005) Expression of truncated latent TGF-beta-binding protein modulates TGF-beta signaling. J Cell Sci 118:2177-87