TY - JOUR
T1 - Altered immune response in mice deficient for the G protein-coupled receptor GPR34
AU - Liebscher, Ines
AU - Müller, Uwe
AU - Teupser, Daniel
AU - Engemaier, Eva
AU - Engel, Kathrin M.Y.
AU - Ritscher, Lars
AU - Thor, Doreen
AU - Sangkuhl, Katrin
AU - Ricken, Albert
AU - Wurm, Antje
AU - Piehler, Daniel
AU - Schmutzler, Sandra
AU - Fuhrmann, Herbert
AU - Albert, Frank W.
AU - Reichenbach, Andreas
AU - Thiery, Joachim
AU - Schöneberg, Torsten
AU - Schulz, Angela
PY - 2011/1/21
Y1 - 2011/1/21
N2 - The X-chromosomal GPR34 gene encodes an orphan Gi protein-coupled receptor that is highly conserved among vertebrates. To evaluate the physiological relevance of GPR34, we generated a GPR34-deficient mouse line. GPR34-deficient mice were vital, reproduced normally, and showed no gross abnormalities in anatomical, histological, laboratory chemistry, or behavioral investigations under standard housing. Because GPR34 is highly expressed in mononuclear cells of the immune system, mice were specifically tested for altered functions of these cell types. Following immunization with methylated BSA, the number of granulocytes and macrophages in spleens was significantly lower in GPR34-deficient mice as in wild-type mice. GPR34-deficient mice showed significantly increased paw swelling in the delayed type hypersensitivity test and higher pathogen burden in extrapulmonary tissues after pulmonary infection with Cryptococcus neoformans compared with wild-type mice. The findings in delayed type hypersensitivity and infection tests were accompanied by significantly different basal and stimulated TNF-α, GM-CSF, and IFN-γ levels in GPR34-deficient animals. Our data point toward a functional role of GPR34 in the cellular response to immunological challenges
AB - The X-chromosomal GPR34 gene encodes an orphan Gi protein-coupled receptor that is highly conserved among vertebrates. To evaluate the physiological relevance of GPR34, we generated a GPR34-deficient mouse line. GPR34-deficient mice were vital, reproduced normally, and showed no gross abnormalities in anatomical, histological, laboratory chemistry, or behavioral investigations under standard housing. Because GPR34 is highly expressed in mononuclear cells of the immune system, mice were specifically tested for altered functions of these cell types. Following immunization with methylated BSA, the number of granulocytes and macrophages in spleens was significantly lower in GPR34-deficient mice as in wild-type mice. GPR34-deficient mice showed significantly increased paw swelling in the delayed type hypersensitivity test and higher pathogen burden in extrapulmonary tissues after pulmonary infection with Cryptococcus neoformans compared with wild-type mice. The findings in delayed type hypersensitivity and infection tests were accompanied by significantly different basal and stimulated TNF-α, GM-CSF, and IFN-γ levels in GPR34-deficient animals. Our data point toward a functional role of GPR34 in the cellular response to immunological challenges
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U2 - 10.1074/jbc.M110.196659
DO - 10.1074/jbc.M110.196659
M3 - Article
C2 - 21097509
AN - SCOPUS:78751504780
SN - 0021-9258
VL - 286
SP - 2101
EP - 2110
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 3
ER -