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Transcription_Role of VDR in regulation of genes involved in osteoporosis
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Osteoporosis is a common disease affecting the majority of older women and a
significant minority of older men. It is defined as the gradual reduction in bone
strength with advancing age, particularly in post-menopause women. Osteoporosis is one of
the major and growing health care problems around the world. One of the first genes to be
associated with the common form of osteoporosis is that for the Vitamin D receptor
(VDR ) [1 ]. This gene encodes the nuclear
hormone receptor for vitamin D3 belonging to the family of trans-acting transcriptional
regulatory factors. VDR is activated by active form of
vitamin D - Calcitriol .
Calcitriol is produced in the kidneys via
CYP27B1 by conversion from
Calcifediol .
VDR downstream targets are principally involved in
mineral metabolism. The effects of the vitamin D system on calcium and bone homeostasis
are largely mediated by promoting active intestinal calcium transport via the induction
of the epithelial calcium channel - Transient receptor potential cation channel,
subfamily V, member 6 (TRPV6 ) [2 ]. The
accumulation of intracellular calcium generated by the constitutively open
TRPV6 channels, however, impairs further calcium transport
activity of these channels unless this intracellular free calcium is buffered by proteins
such as Calbindin (CALB1 ). Transcription of
CALB1 is positively regulated by
VDR .
Many essential and typical osteoblast genes are shown to be highly regulated by
VDR including RUNX2 , Type I
collagen alpha 1 (COL1A1 ),
Osteopontin , Osteocalcin .
VDR stimulates Ligand for receptor activator of nuclear
factor kappaB (RANKL )/ Receptor activator of nuclear factor
kappaB (RANK ) -mediated osteoclastogenesis and bone
resorption through up-regulation of RANKL [2 ].
Osteoclast-mediated bone resorption could be inhibited by Osteoprotegerin
(OPG ) which binds RANKL to
prevent association with its receptor [3 ].
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