Ergostane-type steroids from Korean wild mushroom xerula furfuracea that control adipocyte and osteoblast differentiation
- Authors
- Lee, S.R.; Choi, J.H.; Ryoo, R.; Kim, J.-C.; Pang, C.; Kim, S.-H.; Kim, K.H.
- Issue Date
- 2020-11
- Publisher
- Korean Society for Microbiolog and Biotechnology
- Citation
- Journal of Microbiology and Biotechnology, v.30, no.11, pp.1769 - 1776
- Abstract
- As part of our current work to discover structurally and/or biologically novel compounds from Korean wild mushrooms, we isolated five ergostane-type steroids (1-5) from the fruiting bodies of Xerula furfuracea via repeated column chromatographic separations and HPLC purification. The chemical structures of the isolated steroids were shown to be (22E,24R)-24-methylcholesta-4,22-diene-3,6-dione (1), ergosta-7,22-diene-3β,5α,6β-triol (2), ergosta-7,22-diene-3β,5α,6β,9α-tetraol (3), (22E,24R)-5α,8α-epidioxyergosta-6,22-diene-3β-ol-3-O-β-D-glucopyranoside (4), and (22E,24R)-5α,8α-epidioxyergosta-6,9,22-triene-3β-ol-3-O-β-D-glucopyranoside (5) based on comparison of the data regarding their spectroscopic and physical properties with those of previous studies. Notably, this is the first report on the presence of the identified steroids (1-5) in this mushroom. We tested compounds 1?5 to determine their effects on adipogenesis and osteogenesis in the mouse mesenchymal stem cell line C3H10T1/2 and found that compounds 4 and 5 suppressed the differentiation of stem cells into adipocytes. Notably, in addition to its suppressive effect on adipogenesis, compound 5 was also shown to promote the osteogenic differentiation of stem cells. These findings demonstrate that the bioactive compounds isolated might be effective for the treatment of menopause-associated syndromes, such as osteoporosis and obesity, as the isolated compounds were shown to suppress adipogenesis and/or promote osteogenesis of stem cells. ? 2020 Korean Society for Microbiology and Biotechnology. All rights reserved.
- Keywords
- 24 methylcholesta 4,22 diene 3,6 dione; 5alpha,8alpha epidioxyergosta 6,22 diene 3betaol 3o beta dextro glucopyranoside; 5alpha,8alpha epidioxyergosta 6,9,22 triene 3beta ol 3 o beta dextro glucopyranoside; ergosta 7,22 diene 3beta,5alpha,6beta triol; ergosta 7,22 diene 3beta,5alpha,6beta,9alpha tetraol; plant extract; steroid; unclassified drug; Xerula furfuracea extract; adipocyte; adipogenesis; Agaricales; animal cell; Article; bone development; carbon nuclear magnetic resonance; cell differentiation; column chromatography; controlled study; drug identification; drug isolation; drug structure; embryo; high performance liquid chromatography; mesenchymal stem cell; mouse; nonhuman; osteoblast; proton nuclear magnetic resonance; real time polymerase chain reaction; traditional medicine; Xerula furfuracea; traditional medicine; Xerula furfuracea; 24 methylcholesta 4,22 diene 3,6 dione; 5alpha,8alpha epidioxyergosta 6,22 diene 3betaol 3o beta dextro glucopyranoside; 5alpha,8alpha epidioxyergosta 6,9,22 triene 3beta ol 3 o beta dextro glucopyranoside; ergosta 7,22 diene 3beta,5alpha,6beta triol; ergosta 7,22 diene 3beta,5alpha,6beta,9alpha tetraol; plant extract; steroid; unclassified drug; Xerula furfuracea extract; adipocyte; adipogenesis; Agaricales; animal cell; Article; bone development; carbon nuclear magnetic resonance; cell differentiation; column chromatography; controlled study; drug identification; drug isolation; drug structure; embryo; high performance liquid chromatography; mesenchymal stem cell; mouse; nonhuman; osteoblast; proton nuclear magnetic resonance; real time polymerase chain reaction; Adipogenesis; Ergostane-type steroids; Osteogenesis; Physalacriaceae; Xerula furfuracea
- ISSN
- 1017-7825
- URI
- https://pubs.kist.re.kr/handle/201004/117884
- DOI
- 10.4014/JMB.2006.06013
- Appears in Collections:
- KIST Article > 2020
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