1990
DOI: 10.1016/0024-3205(90)90428-t
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Effects of 1, 25-dihydroxyvitamin D3 on the synthesis of DNA and glycosaminoglycans by rat aortic smooth muscle cells in vitro

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Cited by 14 publications
(4 citation statements)
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“…VDR s which are DNA-linked proteins (Mitsuhashi et al 1991) were identified in SMCs in vitro (Kawashima 1987, Merke et al1987, Koh et al 1988. Stimulation of these receptors induce cell proliferation and differentiation in several tissues (Pike 1985, Pols et al 1990, Walters 1992, and there is an increase in DNA synthesis and a decrease in heparan sulfate, a glycosaminoglycan responsible for the inhibition of the proliferation of these cells, allowing multiplication of the SMCs (Koh et al 1990). …”
Section: Discussionmentioning
confidence: 99%
“…VDR s which are DNA-linked proteins (Mitsuhashi et al 1991) were identified in SMCs in vitro (Kawashima 1987, Merke et al1987, Koh et al 1988. Stimulation of these receptors induce cell proliferation and differentiation in several tissues (Pike 1985, Pols et al 1990, Walters 1992, and there is an increase in DNA synthesis and a decrease in heparan sulfate, a glycosaminoglycan responsible for the inhibition of the proliferation of these cells, allowing multiplication of the SMCs (Koh et al 1990). …”
Section: Discussionmentioning
confidence: 99%
“…This active metabolite of vitamin D appears to cause cell cycle arrest and inhibit proliferation of most cell types [3,4]. The mitogenic role of calcitriol in aortal SMCs culture has been previously reported although obtained results are limited and controversial [5][6][7]. The aim of this study was to determine * Corresponding author.…”
Section: Introductionmentioning
confidence: 95%
“…15,16 In particular, 1␣,25-(OH) 2 D 3 has been shown to regulate calcium homeostasis, modulate growth, and increase calcification in smooth muscle cells. [17][18][19] Indeed, the mitogenic role of 1␣,25-(OH) 2 D 3 in VSMCs has been previously reported, 18,20,21 although its effect on the migration has not been investigated. Therefore, the purpose of this study was to determine whether 1␣,25-(OH) 2 D 3 can promote SMC migration, and if so, to determine whether the mechanism is mediated by the genomic or nongenomic effects of VDR.…”
mentioning
confidence: 99%