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. 2020 Sep 26;11:2040622320924159. doi: 10.1177/2040622320924159

Figure 1.

Figure 1.

A simplified schematic representation of the synthesis and metabolism of vitamin D.

7-dehydrocholesterol in the skin is converted to previtamin D3 by UV-B and then is thermally isomerized to vitamin D3. Transport of vitamin D3 from the skin to the liver is mediated by vitamin D binding protein (DBP) where vitamin D3 is hydroxylated at position 25 to 25(OH)D3, DBP then transports 25(OH)D3 to the kidney. 25(OH)D3/DBP is filtered by the glomeruli and 25(OH)D3 is taken up into the tubular cells, following DBP binding to megalin, a transmembrane protein. 25(OH)D3 undergoes a second hydroxylation step by the 1-alpha-hydroxylase Cyp27B1, converting to the active 1α,25 (OH)2D3, while 24 hydroxylase Cyp27A1 converts to 24,25(OH)2D3. Keratinocytes contribute to the 3-epimerase activity, but the exact sites of activity remain unknown. 3epi25(OH)D3 is converted by Cyp27A1 to 24,25(OH)D3 and Cyp27B1 to 1,25(OH)D3, in equal measure. Ergosterol (provitamin D2) is plant-based and is converted to ergocalciferol by UV-B light that then follows the same pathway as vitamin D3 that is depicted with the dotted line * to the liver to form 25(OH)D2 and then transported to the kidney and epimerized to the D2 metabolites.