Abstract
The major circulating form of vitamin D, 25-hydroxyvitamin D3, is synthesized in the liver and serves as a pool of precursor for the dihydroxylated metabolites, l,25(OH)2D3 and 24,25(OH)2D3. l,25(OH)2D3 undoubtedly mediates the primary biological actions classically attributed to vitamin D in the intestine and bone. Although there has accumulated some evidence for a biological role for 24,25(OH)2D3 (1–4), the precise nature of this has not yet been elucidated. The kidney is generally considered to be the major site of synthesis of the dihydroxylated metabolites of vitamin D, although both can also be produced by extrarenal tissues such as the placenta (5,6) or by cells derived from extrarenal tissues such as bone (7,8).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Henry HL, Taylor AN, Norman AW: Effect of the vitamin D metabolites 1,25-dihydroxyvitamin D3 and 24,25-dihydroxyvitamin D3 on chick parathyroid gland size. J. Nutr. 107: 1918–1926, 1977.
Henry HL, Norman AW: Two dihydroxylated vitamin D metabolites are required for normal chick egg hatchability. Science 201: 835–837, 1978.
Corvol M, Ulmann A, Garabedian M: Specific nuclear uptake of 24,25- dihydroxyvitamin, a vitamin D3 metabolite biologically active in cartilage. FEBS Let. 116: 273–276, 1980.
Endo H, Kiyoki M, Kawashima K, Naruchi J, Hashimoto Y: Synergistic stimulatory effect of vitamin D3 metabolites and PTH upon bone formation of chick embryonic femur growing in vitro. Nature 286: 262–264, 1980.
Weisman Y, Harell A, Edelstein S, David M, Spirer Z, Golander A: 1α, 25-Dihydroxyvitamin D3 and 24,25-dihydroxyvitamin D3 in vitro synthesis by human decidua and placenta. Nature 281: 317–319, 1979.
Tanaka V, Halloran B, Schnoes HK, DeLaca HF: In vitro production of 1,25-dihydroxyvitamin D3 by rat placental tissue. Proc. Natl. Acad. Sci. USA 76: 5033–5035, 1979.
Howard GA, Turner TR, Sherrard D, Baylink DJ: Human bone cells in culture metabolize 25-OH-D3 to 1,25-dihydroxyvitamin D3 and 24,25- dihydroxyvitamin D3. J. Biol. Chem. 256: 77 38–7740, 1981.
Turner RT, Puzas JE, Forte MD, Lester GE, Gray TK, Howard GA, Baylink DJ: In vitro synthesis of 1α,25-dihydroxycholecalciferol by isolated calvarial cells. Proc. Natl. Acad. Sci. USA 77: 5720–5724, 1980.
Fraser DR: Regulation of the metabolism of vitamin D. Phys. Rev. 60: 551–613, 1980.
Henry H, Norman AW: Renal 25-hydroxyvitamin D3-1-hydroxylase: involvement of cytochrome P-450 and other properties. J. Biol. Chem. 249: 7529–7535, 1974.
Ghazarian JG, Jefcoate CR, Knutson JC, Orme-Johnson WH, DeLuca HF: Mitochondrial cytochrome P-450: A component of chick kidney 25- hydroxycholecalciferol-l-hydroxylase. J. Biol. Chem. 249: 3026–3033, 1974.
Pedersen JI, Ghazarian JG, Orme-Johnson NR, DeLuca HF: Isolation of chick renal mitochondrial ferredoxin active in the 25-hydroxyvitamin D3-lα-hydroxylase system. J. Biol. Chem. 251:3933–3941,1976.
Fraser DR, Kodicek E: Unique biosynthesis by kidney of a biologically active vitamin D metabolite. Nature 228: 764–766, 1970.
Henry HL, Midgett RJ, Norman AW: Regulation of 25-hydroxyvitamin D3-1-hydroxylase, in vivo. J. Biol. Chem. 249: 7584–7592, 1974.
Colston KW, Evans IMA, Spelsberg T, Maclntyre I: Feedback regulation of vitamin D metabolism by 1,25-dihydroxycholecalciferol. Biochem. J. 164: 83–89, 1977.
Castillo L, Tanaka Y, DeLuca HF: Parathyroid hormone is not involved in 1,25-dihydroxyvitamin D regulation of 25-hydroxyvitamin D metabolism in vivo. Biochem. Biophys. Res. Comm. 100: 1332–1336, 1981.
Henry HL: Metabolism of 25-hydroxyvitamin D3 by primary cultures of chick kidney cells. Biochem. Biophys. Res. Comm. 74: 768–774, 1977.
Henry H: Regulation of the hydroxylation of 25-hydroxyvitamin D3 in vivo and in primary cultures of chick kidney cells. J. Biol. Chem. 254: 2722–2729, 1979.
Trechsel U, Bonjour J-P, Fleisch H: Regulation of the metabolism of 25-hydroxyvitamin D3 in primary cultures of chick kidney cells. J. Clin. Invest. 64: 206–217, 1979.
Spanos E, Barrett DI, Chong KT, Maclntyre I: Effect of oestrogen and 1,25-dihydroxycholecalciferol on 25-hydroxycholecalciferol metabolism in primary chick kidney cell culture. Biochem. J. 724: 231–236, 1978.
Omdahl JL, Hunsaker LA, Evan AP, Torrez P: In vitro regulation of kidney 25-hydroxyvitamin D3-hydroxylase enzyme activities by vitamin D3 metabolites. J. Biol. Chem. 255: 7460–7466, 1980.
Kumar R, Harnden D, DeLuca HF: Metabolism of 1,25-dihydroxyvitamin D3: Evidence for side chain oxidation. Biochemistry 15: 2420–2423, 1976.
Gray RW, Caldas A, Wilz DR, Leraann J, DeLuca HF: The metabolism and excretion of 3H-1,25(OH)2D3 in healthy adults. J. Clin. Endocrinol. Metab. 46: 756–765, 1978.
Ohnuma N, Norman AW: Studies on the metabolism of calciferol. XX. Identification of a new C-23-oxidation pathway of metabolism of 1,25-dihydroxyvitamin D3 present in intestine and kidney. J. Biol. Chem. 257: 8261–8271, 1982.
Simpson RU, Franceschi RT, DeLuca HF: Characterization of a specific, high affinity binding macromolecule for 1α,25-dihydroxy-vitamin D3 in cultured chick kidney cells. J. Biol. Chem. 255: 10160–10166, 1980.
Henry H: Regulation of 25-hydroxyvitamin D metabolism in kidney cell cultures. Hormonal Control of Calcium Metabolism. Proceedings of the Vllth International Conference on Calcium Regulating Hormones, Excerpta Medica, 1981, p 202–211.
Colston KW, Feldman D: 1,25-Dihydroxyvitamin D3 receptors and functions in cultured pig kidney cells (LLC P1). J. Biol. Chem. 257: 2504–2508, 1982.
Garabedian M, Holick MF, DeLuca HF, Boyle IT: Control of 25-hydroxycholecalciferol metabolism by parathyroid glands. Proc. Natl. Acad. Sci. USA 69: 1673–1676, 1972.
Fraser DR, Kodicek E: Regulation of 25-hydroxycholecalciferol-1- hydroxylase activity by parathyroid hormone. Nature, London 241: 163–165, 1973.
Rasmussen H, Wong M, Bikle D, Goodman DBP: Hormonal control of the renal conversion of 25-hydroxycholecalciferol to 1,25-dihydroxycholecalciferol. J. Clin. Invest. 51: 2502–2504, 1972.
Henry HL, Midgett RJ, Norman AW: Regulation of 25-hydroxyvitamin Di-l-hydroxylase, in vivo. J. Biol. Chem. 249: 7584–7592, 1974.
Booth BD, Tsai HC, Morris Jr C: Parathyroidectomy reduces 25-hydroxyvitamin D3-1α-hydroxylase activity in the hypocalcemic vitamin D- deficient chick. J. Clin. Invest. 60: 1314–1320, 1977.
Calante LH, Colston KW, Evans IMA, Byfield PGH, Matthews EW, Maclntyre I: The regulation of vitamin D metabolism. Nature 244: 438–440, 1973.
Baksi SN, Kenny AD: Acute effect of parathyroid extract on renal vitamin D hydroxylases in Japanese quail. Pharmacology 18: 169–174, 1979.
Howard GA, Turner RT, Bottemiller BL, Rader JI: Serum-free culture of Japanese quail kidney cells: Regulation of vitamin D metabolism. Biochia. Biophys. Acta 587: 495–506, 1979.
Juan D, DeLuca HF: The regulation of 24,25-dihydroxyvitamin D3 production in cultures of monkey kidney cells. Endocrinology 101: 1184–1193, 1977.
Spanos E, Brown DJ, Maclntyre I: Regulation of 25-OH-D3 metabolism by parathyroid hormone in primary chick kidney cell cultures. FEBS Let. 105: 31–34, 1979.
Henry H: Insulin permits parathyroid hormone stimulation of 1,25- dihydroxyvitamin D3 production in cultured kidney cells. Endocrinology 108: 733–735, 1981.
Henry H: Insulin permits parathyroid hormone stimulation of 1,25- dihydroxyvitamin D3 production in cultured kidney cells. Endocrinology 108: 733–735, 1981.
Rudack-Garcia D, Henry H: Effect of vitamin D status on cyclic AMP dependent protein kinase and its heat stable inhibitor in chick kidney. J. Biol. Chem. 256: 10781–10785, 1981.
Rudack-Garcia D, Henry H: Effect of vitamin D status on cyclic AMP dependent protein kinase and its heat stable inhibitor in chick kidney. J. Biol. Chem. 256: 10781–10785, 1981.
Kawashima H, Torikai S, Kurokawa K: Calcitonin selectively stimulates 25-hydroxyvitamin D3-a-hydroxylase in proximal straight tubule of rat kidney. Nature 291: 327–329, 1981.
Larkins RC, MacAules SJ, Rapoport A, Martin TJ, Tullock BR, Byfield PCH, Matthews EW, Maclntyre I: Effects of nucleotides, hormones, ions, and 1,25-dihydroxycholecalciferol on 1,25-dihydroxycholecalciferol production in isolated chick renal tubules. Clin. Sci. Mol. Med. 46: 569–582, 1974.
Tanaka Y, Castillo L, DeLuca HF: Control of renal vitamin D hydroxylases in birds by sex hormones. Proc. Natl. Acad. Sci. USA 73: 2701–2705, 1976.
Castillo L, Tanaka Y, DeLuca HF, Sunde ML: The stimulation of 25- hydroxyvitamin D3-1α-hydroxylase by estrogen. Arch. Biochem. Biophys. 179: 211–217, 1977.
Baksi SN, Kenny AD: Vitamin D metabolism in Japanese quail: gonadal hormones and dietary calcium effects. Am. J. Physiol. 234: E622–E628, 1978.
Baksi SN, Kenny AD: Acute effect of estradiol on the renal vitamin D hydroxylases in Japanese quail. Biochem. Pharmacol. 27: 2765–2768, 1978.
Pike JW, Spanos E, Colston KW, Maclntyre I, Haussler MR: Influence of estrogen on renal vitamin D hydroxylases and serum l,25(OH)2D3 in chicks. An. J. Physiol. 235: E338–E343, 1978.
Henry HL: 25-OH-D3 metabolism in kidney cell cultures: Lack of a direct effect of estradiol. Am. J. Physiol. 240:E119–E124, 1981.
Bouillon R, Van Assche FA, Van Baelen H, Heyns W, DeMoor P: Influence of the vitamin D-binding protein on the serum concentration of 1,25-dihydroxyvitamin D3. J. Clin. Invest. 67: 589–596, 1981.
Spanos E, Brown DJ, Stevenson JC, MacIntyre I: Stimulation of 1,25-dihydroxycholecalciferol production by prolactin and related peptides in intact renal cell preparations in vitro Biochiro. Biophys. Acta 672: 7–15, 1981.
Cray RW: Control of plasma 1,25(OH)2-vitamin D concentrations by calcium and phosphorus in the rat: Effects of hypophysectoay. Calcif. Tiss. Int. 33: 485–488, 1981.
Bikle DD, Rasmussen H: The ionic control of 1,25-dihydroxyvitanin D3 production in isolated chick renal tubules. J. Clin. Invest. 55: 292–298, 1975.
Spanos E, Freake H, MacAuley SJ, Maclntyre I: Regulation of vitamin D metabolism by calcium and phosphate ions in isolated renal tubules. Biochem. J. 196: 193–197, 1981.
Trechsel U, Taylor CM, Bonjour J-P, Fleisch H: Influence of prostaglandins and of cyclic nucleotides on the metabolism of 25-hydroxyvitamin D3 in primary chick kidney cell culture. Biochem. Biophys. Res. Comm. 93: 1210–1215, 1980.
Wark JD, Larkins RC, Eisman JA, Wilson KR: Regulation of 25-hydroxyvitamin D3-1α-hydroxylase in chick isolated renal tubules: Effects of prostaglandin E2, fursemide and acetylsalicylic acid. J. Clin. Sci. 61: 53–59, 1981.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 Martinus Nijhoff Publishing, Boston/The Hague/Dordrecht/Lancaster
About this chapter
Cite this chapter
Henry, H.L. (1984). Regulation of the Synthesis of 1,25-Dihydroxyvitamin D3 and 24,25- Dihydroxyvitamin D3 in Kidney Cell Culture. In: Kumar, R. (eds) Vitamin D. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2839-1_5
Download citation
DOI: https://doi.org/10.1007/978-1-4613-2839-1_5
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4612-9793-2
Online ISBN: 978-1-4613-2839-1
eBook Packages: Springer Book Archive