TY - JOUR
T1 - No evidence for a bone phenotype in GPRC6A knockout mice under normal physiological conditions
AU - Wellendorph, Petrine
AU - Johansen, Lars Dan
AU - Jensen, Anders Asbjørn
AU - Casanova, Emilio
AU - Gassmann, Martin
AU - Deprez, Pierre
AU - Clément-Lacroix, Philippe
AU - Bettler, Bernhard
AU - Bräuner-Osborne, Hans
PY - 2009
Y1 - 2009
N2 - GPRC6A is a seven transmembrane receptor mediating signaling by a wide range of L-alpha-amino-acids, a signaling augmented by the divalent cations Ca2+ and Mg2+. GPRC6A transcripts are detected in numerous mammalian tissues, but the physiological role of the receptor is thus far elusive. Analogously to the closely related calcium-sensing receptor, GPRC6A has been proposed to function as a metabolic sensor of Ca2+ and amino acids in bone and other tissues. In the present study, we have generated the first GPRC6A knockout mice and studied their phenotype with particular focus on bone homeostasis. The generated GPRC6A knockout mice are viable and fertile, develop normally and exhibit no significant differences in body weight compared to wild type littermates. Assessment of bone mineral density, histomorphometry and bone metabolism demonstrated no significant differences between 13-week-old knockout and wild type mice. In conclusion, our data do not support a role for GPRC6A in normal bone physiology.
AB - GPRC6A is a seven transmembrane receptor mediating signaling by a wide range of L-alpha-amino-acids, a signaling augmented by the divalent cations Ca2+ and Mg2+. GPRC6A transcripts are detected in numerous mammalian tissues, but the physiological role of the receptor is thus far elusive. Analogously to the closely related calcium-sensing receptor, GPRC6A has been proposed to function as a metabolic sensor of Ca2+ and amino acids in bone and other tissues. In the present study, we have generated the first GPRC6A knockout mice and studied their phenotype with particular focus on bone homeostasis. The generated GPRC6A knockout mice are viable and fertile, develop normally and exhibit no significant differences in body weight compared to wild type littermates. Assessment of bone mineral density, histomorphometry and bone metabolism demonstrated no significant differences between 13-week-old knockout and wild type mice. In conclusion, our data do not support a role for GPRC6A in normal bone physiology.
KW - Former Faculty of Pharmaceutical Sciences
U2 - 10.1677/JME-08-0149
DO - 10.1677/JME-08-0149
M3 - Journal article
C2 - 19103720
SN - 0952-5041
VL - 42
SP - 215
EP - 223
JO - Journal of Molecular Endocrinology
JF - Journal of Molecular Endocrinology
IS - 3
ER -