Biology:Cholesterol 25-hydroxylase

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Short description: Class of enzymes
Cholesterol 25-hydroxylase
Identifiers
EC number1.14.99.38
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum

In enzymology, a cholesterol 25-hydroxylase (EC 1.14.99.38) is an enzyme that catalyzes the chemical reaction

cholesterol + AH2 + O2 [math]\displaystyle{ \rightleftharpoons }[/math] 25-hydroxycholesterol + A + H2O

The 3 substrates of this enzyme are cholesterol, an electron acceptor AH2, and O2, whereas its 3 products are 25-hydroxycholesterol (25HC), the reduction product A, and H2O.

This enzyme belongs to the family of oxidoreductases, specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen. The oxygen incorporated need not be derive from O miscellaneous. The systematic name of this enzyme class is cholesterol, hydrogen-donor:oxygen oxidoreductase (25-hydroxylating). This enzyme is also called cholesterol 25-monooxygenase.

Transcripts for this enzyme have been identified in macrophages from the testis.

CH25H is an interferon-stimulated gene, and its primary product 25HC may have broad-spectrum antiviral activity, demonstrated in mice against HIV, ebola, Nipah virus, Rift Valley Fever virus, and SARS-CoV-2. Specifically, 25HC blocks membrane fusion between the cell and virus, and may "implicate membrane-modifying oxysterols as potential antiviral therapeutics.” Recently, upregulation of CH25H has been shown to play a role in effectively restricting infection of lung epithelial cells with SARS-Cov-2 through its enzymatic product, 25HC, which depletes accessible membrane cholesterol so that the virus is unable to achieve fusion with the cell membrane necessary for entry and infection.[1]

It has been proposed, based on experimental research in both mice and human cell culture, that 25HC is a potent senolytic. Further research needs to elaborate on this research and reveal its true significance to aging.[2]

References

  1. "Cholesterol 25-Hydroxylase inhibits SARS-CoV-2 and other coronaviruses by depleting membrane cholesterol". The EMBO Journal 39 (21): e106057. November 2020. doi:10.15252/embj.2020106057. PMID 32944968. 
  2. Limbad, Chandani; Doi, Ryosuke; McGirr, Julia; Ciotlos, Serban; Perez, Kevin; Clayton, Zachary S.; Daya, Radha; Seals, Douglas R. et al. (February 2022). "Senolysis induced by 25-hydroxycholesterol targets CRYAB in multiple cell types" (in en). iScience 25 (2): 103848. doi:10.1016/j.isci.2022.103848. PMID 35198901. 

Further reading

  • "cDNA cloning of mouse and human cholesterol 25-hydroxylases, polytopic membrane proteins that synthesize a potent oxysterol regulator of lipid metabolism". The Journal of Biological Chemistry 273 (51): 34316–27. December 1998. doi:10.1074/jbc.273.51.34316. PMID 9852097. 
  • "25-hydroxycholesterol is produced by testicular macrophages during the early postnatal period and influences differentiation of Leydig cells in vitro". Biology of Reproduction 66 (5): 1336–41. May 2002. doi:10.1095/biolreprod66.5.1336. PMID 11967195. 
  • "Testosterone regulates 25-hydroxycholesterol production in testicular macrophages". Biology of Reproduction 67 (5): 1435–8. November 2002. doi:10.1095/biolreprod.102.007575. PMID 12390873. 
  • "Resonance Raman evidence for an Fe-O-Fe center in stearoyl-ACP desaturase. Primary sequence identity with other diiron-oxo proteins". Biochemistry 33 (43): 12776–86. November 1994. doi:10.1021/bi00209a008. PMID 7947683. 
  • "The enzymes, regulation, and genetics of bile acid synthesis". Annual Review of Biochemistry 72: 137–74. 2003. doi:10.1146/annurev.biochem.72.121801.161712. PMID 12543708.