A key finding supporting a causal role of the immune system in the pathogenesis of hypertension is the observation that knockout mice on a C57Bl/6J background (B6.Rag1), which lack functional B and T cells, develop a much milder hypertensive response to Ang II (angiotensin II) than control C57Bl/6J mice. Here, we report that we never observed any Ang II resistance of B6.Rag1 mice purchased directly from the Jackson Laboratory as early as 2009. B6.Rag1 mice displayed nearly identical blood pressure increases monitored via radiotelemetry and hypertensive end-organ damage in response to different doses of Ang II and different levels of salt intake (0.02%, 0.3%, and 3% NaCl diet). Similarly, restoration of T-cell immunity by adoptive cell transfer did not affect the blood pressure response to Ang II in B6.Rag1 mice. Full development of the hypertension-resistant phenotype in B6.Rag1 mice appears to depend on the action of yet unidentified nongenetic modifiers in addition to the absence of functional T cells.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1161/HYPERTENSIONAHA.119.13773 | DOI Listing |
Immunohorizons
October 2018
Department of Immunobiology, University of Arizona, Tucson, AZ 85724.
, isolated from the oral cavity of wild-caught mice, does not colonize most inbred mouse strains. does weakly (50%) colonize C57BL/6J (B6) mice but readily colonizes CAST/EiJ (CAST) mice. In this study, we examined whether differences in the CAST and B6 host response could elucidate mechanisms governing colonization.
View Article and Find Full Text PDFHepatology
October 2016
Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute-Frederick, Frederick, MD.
Mucosal Immunol
September 2014
Division of Nephrology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Induced Forkhead box P3-positive (Foxp3(+)) T-regulatory cells (iTregs) are essential to gastrointestinal immune homeostasis, and loss of the ability to develop iTregs may lead to autoimmune colitis. We previously showed a role for sirtuin-1 (Sirt1) in control of Treg function and hypothesized that targeting of Sirt1 might enhance iTreg development and thereby represent a potential therapy for inflammatory bowel disease (IBD). We adoptively transferred CD4(+)CD25(-)Foxp3(-) T effector (TE) cells from wild-type (WT) (C57BL/6) or fl-Sirt1/CD4cre mice into B6/Rag1(-/-) mice and monitored the mice until they lost 10-15% of their weight.
View Article and Find Full Text PDFMelanoma Res
April 2014
aCellular Communication Laboratory, Center for Molecular Studies of the Cell (CEMC), Advanced Center for Chronic Diseases (ACCDiS), School of Medicine, Universidad de Chile bDepartment of Surgery, Hospital Clinico Universidad de Chile cAndes Biotechnologies, Fundación Ciencias y Vida dSchool of Biological Sciences, Universidad Andres Bello, Santiago, Chile eDivision of Biomedical Sciences, St. George's, University of London, London, UK fFreie Universität Berlin - Institut für Pharmakologie, Berlin, Germany.
Melanomas are highly lethal skin tumours that are frequently treated by surgical resection. However, the efficacy of such procedures is often limited by tumour recurrence and metastasis. Caveolin-1 (CAV1) has been attributed roles as a tumour suppressor, although in late-stage tumours, its presence is associated with enhanced metastasis.
View Article and Find Full Text PDFJ Heart Lung Transplant
September 2012
Department of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, Denver, CO, USA.
Background: Previous studies have shown that acute CD4 T-cell-mediated cardiac allograft rejection requires donor major histocompatibility complex (MHC) Class II expression and can be independent of "indirect" antigen presentation. However, other studies suggested that indirect antigen presentation to CD4 T cells may play a primary role in cellular xenograft immunity. Thus, the relative roles of direct/indirect CD4 T cell reactivity against cardiac xenografts are unclear.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!