Caren M. Villano
Rutgers University
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Featured researches published by Caren M. Villano.
Toxicological Sciences | 2008
Jedd M. Hillegass; Caren M. Villano; Keith R. Cooper; Lori A. White
Teratogenic effects are observed following long-term administration of glucocorticoids, although short-term glucocorticoid therapy is still utilized to reduce fetal mortality, respiratory distress syndrome, and intraventricular hemorrhage in preterm infants. However, the mechanism of glucocorticoid-induced teratogenicity is unknown. We hypothesize that glucocorticoid-induced teratogenesis is mediated through the glucocorticoid receptor (GR) and results from altering the expression and activity of the matrix metalloproteinases (MMPs). During embryogenesis, degradation of the extracellular matrix to allow for proper cellular migration and tissue organization is a tightly regulated process requiring appropriate temporal and spatial expression and activity of the MMPs. Studies have demonstrated that MMP gene expression can be either inhibited or induced by glucocorticoids in a variety of model systems. Using the zebrafish (Danio rerio) as a model of development, the data presented here demonstrate that embryonic exposure to the glucocorticoids dexamethasone or hydrocortisone increased expression of two gelatinases, MMP-2 ( approximately 1.5-fold) and MMP-9 (7.6- to 9.0-fold), at 72 h postfertilization (hpf). Further, gelatinase activity was increased approximately threefold at 72 hpf following glucocorticoid treatment, and changes in craniofacial morphogenesis were also observed. Cotreatment of zebrafish embryos with each glucocorticoid and the GR antagonist RU486 resulted in attenuation of glucocorticoid-induced increases in MMP expression (52-84% decrease) and activity (41-94% decrease). Furthermore, the abnormal craniofacial phenotype observed following glucocorticoid exposure was less severe following RU486 cotreatment. These studies demonstrate that in the embryonic zebrafish, dexamethasone, and hydrocortisone alter expression and activity of MMP-2 and -9, and suggest that these increases may be mediated through the GR.
Biological Chemistry | 2006
Jedd M. Hillegass; Kyle A. Murphy; Caren M. Villano; Lori A. White
Abstract The aryl hydrocarbon receptor (AhR) was identified as the receptor for polycyclic aromatic hydrocarbons and related compounds. However, novel data indicate that the AhR binds a variety of unrelated endogenous and exogenous compounds. Although AhR knockout mice demonstrate that this receptor has a role in normal development and physiology, the function of this receptor is still unclear. Recent evidence suggests that AhR signaling also alters the expression of genes involved in matrix metabolism, specifically the matrix metalloproteinases (MMPs). MMP expression and activity is critical to normal physiological processes that require tissue remodeling, as well as in mediating the progression of a variety of diseases. MMPs not only degrade structural proteins, but are also important mediators of cell signaling near or at the cell membrane through exposure of cryptic sites, release of growth factors, and cleavage of receptors. Therefore, AhR modulation of MMP expression and activity may be critical, not only in pathogenesis, but also in understanding the endogenous function of the AhR. In this review we will examine the data indicating a role for the AhR-signaling pathway in the regulation of matrix remodeling, and discuss potential molecular mechanisms.
Journal of Cosmetic Dermatology | 2010
Leonel E. Rojo; Caren M. Villano; Gili Joseph; Barbara Schmidt; Vladimir Shulaev; Joel L. Shuman; Mary Ann Lila; Ilya Raskin
Background Cell migration, angiogenesis, inflammation, and extracellular matrix remodeling are key events in wound healing. Natural products, including fatty acids (FAs), can accelerate wound healing by modulating the aforementioned events.
Journal of Cosmetic Dermatology | 2010
Leonel E. Rojo; Caren M. Villano; Gili Joseph; Barbara Schmidt; Vladimir Shulaev; Joel L Shuman; Mary Ann Lila; Ilya Raskin
Background Cell migration, angiogenesis, inflammation, and extracellular matrix remodeling are key events in wound healing. Natural products, including fatty acids (FAs), can accelerate wound healing by modulating the aforementioned events.
Journal of Cosmetic Dermatology | 2010
Leonel E. Rojo; Caren M. Villano; Gili Joseph; Barbara Schmidt; Vladimir Shulaev; Joel L. Shuman; Mary Ann Lila; Ilya Raskin
Background Cell migration, angiogenesis, inflammation, and extracellular matrix remodeling are key events in wound healing. Natural products, including fatty acids (FAs), can accelerate wound healing by modulating the aforementioned events.
Toxicology and Applied Pharmacology | 2006
Caren M. Villano; Kyle A. Murphy; A.M. Akintobi; Lori A. White
Journal of Biological Chemistry | 2004
Kyle A. Murphy; Caren M. Villano; Ruth Dorn; Lori A. White
Toxicological Sciences | 2007
Jedd M. Hillegass; Caren M. Villano; Keith R. Cooper; Lori A. White
Toxicology and Applied Pharmacology | 2007
A.M. Akintobi; Caren M. Villano; Lori A. White
Toxicology and Applied Pharmacology | 2006
Caren M. Villano; Lori A. White