4 results match your criteria: "USA. Veterans Affairs Hospital[Affiliation]"

Dos and Don'ts in the Management of Cirrhosis: A View from the 21st Century.

Am J Gastroenterol

July 2018

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, MI, USA. Institute for Healthcare Policy and Innovation, University of Michigan, Ann Arbor, MI, USA. Veterans Affairs Hospital, Ann Arbor, MI, USA.

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Transcription Factor KLF2 in Dendritic Cells Downregulates Th2 Programming via the HIF-1α/Jagged2/Notch Axis.

mBio

June 2016

Division of Infectious Diseases, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA Veterans Affairs Hospital, Cincinnati, Ohio, USA

Unlabelled: The adaptive immune response is tightly regulated by complex signals in dendritic cells (DCs). Although Th2 polarization is dictated by defined functional DC subsets, the molecular factors that govern the amplitude of these responses are not well understood. Krüppel-like factor 2 (KLF2) is a transcription factor that negatively regulates the activation of numerous immune cells in response to stimuli.

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Cdc42 regulates epithelial cell polarity and cytoskeletal function during kidney tubule development.

J Cell Sci

December 2015

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Cancer Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

The Rho GTPase Cdc42 regulates key signaling pathways required for multiple cell functions, including maintenance of shape, polarity, proliferation, migration, differentiation and morphogenesis. Although previous studies have shown that Cdc42 is required for proper epithelial development and maintenance, its exact molecular function in kidney development is not well understood. In this study, we define the specific role of Cdc42 during murine kidney epithelial tubulogenesis by deleting it selectively at the initiation of ureteric bud or metanephric mesenchyme development.

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Metal-mediated modulation of streptococcal cysteine protease activity and its biological implications.

Infect Immun

July 2014

Department of Molecular Genetics, Biochemistry and Microbiology, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA Department of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, North Dakota, USA Veterans Affairs Hospital, Cincinnati, Ohio, USA

Streptococcal cysteine protease (SpeB), the major secreted protease produced by group A streptococcus (GAS), cleaves both host and bacterial proteins and contributes importantly to the pathogenesis of invasive GAS infections. Modulation of SpeB expression and/or its activity during invasive GAS infections has been shown to affect bacterial virulence and infection severity. Expression of SpeB is regulated by the GAS CovR-CovS two-component regulatory system, and we demonstrated that bacteria with mutations in the CovR-CovS two-component regulatory system are selected for during localized GAS infections and that these bacteria lack SpeB expression and exhibit a hypervirulent phenotype.

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