This Article Full Text Full Text (PDF) Online  Supplement All Versions of this Article: 2007-0276OCv1 38/3/346    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Yamasaki, M. Articles by Lee, C. G. PubMed PubMed Citation Articles by Yamasaki, M. Articles by Lee, C. G.

P21 Regulates TGF-β₁–Induced Pulmonary Responses via a TNF-–Signaling Pathway

¹ Section of Pulmonary and Critical Care Medicine, and ² Department of Pathology, Yale University School of Medicine, New Haven, Connecticut; and ³ Pathology and Laboratory Medicine Service, VA-CT Health Care System, West Haven, Connecticut

Correspondence and requests for reprints should be addressed to Chun Geun Lee, M.D., Ph.D., Assistant Professor of Medicine, Section of Pulmonary and Critical Care Medicine, Yale University School of Medicine, Department of Internal Medicine, 300 Cedar Street – S425A TAC, P.O. Box 208057, New Haven, CT 06520-8057. E-mail: chungeun.lee{at}yale.edu

Transforming growth factor (TGF)-β₁ is an essential regulatory cytokine that has been implicated in the pathogenesis of diverse facets of the injury and repair responses in the lung. The types of responses that it elicits can be appreciated in studies from our laboratory that demonstrated that the transgenic (Tg) overexpression of TGF-β₁ in the murine lung causes epithelial apoptosis followed by fibrosis, inflammation, and parenchymal destruction. Because a cyclin-dependent kinase inhibitor, p21, is a key regulator of apoptosis, we hypothesized that p21 plays an important role in the pathogenesis of TGF-β₁–induced tissue responses. To test this hypothesis we evaluated the effect of TGF-β₁ on the expression of p21 in the murine lung. We also characterized the effects of transgenic TGF-β₁ in mice with wild-type and null mutant p21 loci. These studies demonstrate that TGF-β₁ is a potent stimulator of p21 expression in the epithelial cells and macrophages in the murine lung. They also demonstrate that TGF-β₁–induced lung inflammation, fibrosis, myofibroblast accumulation, and alveolar destruction are augmented in the absence of p21, and that these alterations are associated with exaggerated levels of apoptosis and caspase-3 activation. Finally, our studies further demonstrated that TGF-β₁ induces p21 via a TNF-–signaling pathway and that p21 is a negative modulator of TGF-β₁–induced TNF- expression. Collectively, our studies demonstrate that p21 regulates TGF-β₁–induced apoptosis, inflammation, fibrosis, and alveolar remodeling by interacting with TNF-–signaling pathways.

Key Words: TGF-β • p21 • apoptosis • fibrosis • emphysema

CLINICAL RELEVANCE This is the first report directly demonstrating the in vivo role of p21 in fibrosis and alveolar destruction in association with TGF-β1 expression. Intervention of p21 has therapeutic potential for the fibrotic and destructive lung disease as well.