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PMID: 11545681 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

1,25-Dihydroxyvitamin D3 increases the expression of the CaT1 epithelial calcium channel in the Caco-2 human intestinal cell line.

BMC physiology ·Vol. 1 ·2001-00-00 ·Pages 11

Wood RJ, Tchack L, Taparia S

Abstract

The active hormonal form of vitamin D (1,25-dihydroxyvitamin D) is the primary regulator of intestinal calcium absorption efficiency. In vitamin D deficiency, intestinal calcium absorption is low leading to an increased risk of developing negative calcium balance and bone loss. 1,25-dihydroxyvitamin D has been shown to stimulate calcium absorption in experimental animals and in human subjects. However, the molecular details of calcium transport across the enterocyte are not fully defined. Recently, two novel epithelial calcium channels (CaT1/ECaC2 and ECaC1/CaT2) have been cloned and suggested to be important in regulating intestinal calcium absorption. However, to date neither gene has been shown to be regulated by vitamin D status. We have previously shown that 1,25-dihydroxyvitamin stimulates transcellular calcium transport in Caco-2 cells, a human intestinal cell line. In the current study, we have demonstrated that Caco-2 cells express low but detectable levels of CaT1 mRNA in the absence of 1,25-dihydroxyvitamin D treatment. CaT1 mRNA expression is rapidly up regulated (4-fold increase at 4 h and 10-fold at 24 h) by treatment with 1,25-dihydroxyvitamin D (10(-7) moles/L). Moreover, the increase in CaT1 mRNA expression preceded by several hours the vitamin D induction of calbindin D9K, a putative cytosolic calcium transport protein. These observations are the first to demonstrate regulation of CaT1 expression by vitamin D and are consistent with a new model of intestinal calcium absorption wherein vitamin D-mediated changes in brush border membrane CaT1 levels could be the primary gatekeeper regulating homeostatic modulation of intestinal calcium absorption efficiency.

MeSH Terms
Caco-2 Cells Calbindins Calcitriol/pharmacology Calcium Channels/biosynthesis,genetics Enterocytes/drug effects,metabolism Gene Expression Regulation Humans Kinetics RNA, Messenger/metabolism S100 Calcium Binding Protein G/biosynthesis,genetics TRPV Cation Channels Up-Regulation
Chemicals
Calbindins Calcium Channels RNA, Messenger S100 Calcium Binding Protein G S100G protein, human TRPV Cation Channels TRPV6 channel Calcitriol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wood R J
Mineral Bioavailability Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111, USA. rwood@hnrc.tufts.edu
Tchack L
Taparia S
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Article Info
Journal
BMC physiology
Abbr.
BMC Physiol
ISSN
1472-6793
Published
2001-00-00
Epub
2001-00-17
Pages
11
Language
English
Region
England
NLM ID
101088687
PMCID
PMC55338
Subset
IM
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