Phenotype of a Calbindin-D9k Gene Knockout Is Compensated for by the Induction of Other Calcium Transporter Genes in a Mouse Model
Open Access
- 1 December 2007
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Bone and Mineral Research
- Vol. 22 (12) , 1968-1978
- https://doi.org/10.1359/jbmr.070801
Abstract
CaBP‐9k may be involved in the active calcium absorption and embryo implantation. Although we generated CaBP‐9k KO mice to explore its function, no distinct phenotypes were observed in these KO mice. It can be hypothesized that TRPV5 and 6 and plasma membrane calcium ATPase 1b may play a role in the regulation of calcium transport to compensate CaBP‐9k deficiency in its KO model. Introduction: Active calcium transport in the duodenum and kidney is carried in three steps: calcium entry through epithelial Ca2+ channels (TRPV5 and TRPV6), buffering and/or transport by calbindin‐D9k (CaBP‐9k) and ‐D28k (CaBP‐28k), and extrusion through the plasma membrane calcium ATPase 1b (PMCA1b) and sodium/calcium exchanger 1. Although the molecular mechanism of calcium absorption has been studied using knockouts (KOs) of the vitamin D receptor and CaBP‐28k in animals, the process is not fully understood. Materials and Methods: We generated CaBP‐9k KO mice and assessed the phenotypic characterization and the molecular regulation of active calcium transporting genes when the mice were fed different calcium diets during growth. Results: General phenotypes showed no distinct abnormalities. Thus, the active calcium transport of CaBP‐9k–null mice proceeded normally in this study. Therefore, the compensatory molecular regulation of this mechanism was elucidated. Duodenal TRPV6 and CaBP‐9k mRNA of wildtype (WT) mice increased gradually during preweaning. CaBP‐9k is supposed to be an important factor in active calcium transport, but its role is probably compensated for by other calcium transporter genes (i.e., intestinal TRPV6 and PMCA1b) during preweaning and renal calcium transporters in adult mice. Conclusions: Depletion of the CaBP‐9k gene in a KO mouse model had little phenotypic effect, suggesting that its depletion may be compensated for by calcium transporter genes in the intestine of young mice and in the kidney of adult mice.Keywords
This publication has 48 references indexed in Scilit:
- Estrogen Receptor Pathway Is Involved in the Regulation of Calbindin-D9k in the Uterus of Immature RatsToxicological Sciences, 2005
- Compensatory response of IL-1 gene knockout mice after pulmonary infection with Klebsiella pneumoniaeJournal of Medical Microbiology, 2005
- Novel Progestogenic Activity of Environmental Endocrine Disruptors in the Upregulation of Calbindin-D9k in an Immature Mouse ModelToxicological Sciences, 2004
- Effect of Genistein As a Selective Estrogen Receptor Beta Agonist on the Expression of Calbindin-D9k in the Uterus of Immature RatsToxicological Sciences, 2004
- Characterization of a murine renal distal convoluted tubule cell line for the study of transcellular calcium transportAmerican Journal of Physiology-Renal Physiology, 2004
- Complex regulation of Calbindin-D9k in the mouse placenta and extra-embryonic membrane during mid- and late pregnancyMolecular and Cellular Endocrinology, 2004
- Complex Regulation of Calcium-Binding Protein D9k (Calbindin-D9k) in the Mouse Uterus During Early Pregnancy and at the Site of Embryo Implantation1Biology of Reproduction, 2000
- Calbindin-D28k Controls [Ca2+] and Insulin ReleaseJournal of Biological Chemistry, 1999
- Expression of genes involved in calcium absorption in human duodenumEuropean Journal of Clinical Investigation, 1999
- The baboon expresses the calbindin‐D9k gene in intestine but not in uterus and placenta: Implication for conservation of the gene in primatesMolecular Reproduction and Development, 1995