Pathophysiological role of 27-hydroxycholesterol in human diseases.

Dayea Kim, Kwang Min Lee, Chanhee Lee, Yeon Suk Jo, Muradillaeva Shakhnoza Muradillaevna, Jae Ho Kim, Jong Hyuk Yoon, Parkyong Song

Journal: Advances in biological regulation 2022;83():100837

PMID: 34774482

Abstract

Oxysterols are oxygenated cholesterol derivatives and important regulators of cholesterol metabolism, lipid homeostasis, the immune system, and membrane fluidity regulation. Although the detailed mechanism of action of oxysterols remains unclear, activation of some nuclear receptors, such as liver X receptor α (LXRα) and RAR-related orphan receptors, have been believed to be critical for the regulation of various physiological processes in multiple tissues. 27-Hydroxycholesterol (27-OHC) is an endogenous oxysterol, which has an intermediate function in cholesterol catabolism to bile acid synthesis. According to previous studies, however, there are opposing opinions on whether 27-OHC activates human LXR. Recently, several studies have shown that 27-OHC can activate or inhibit the function of estrogen receptors ERα and ERβ in a tissue-specific manner, indicating that the understanding of 27-OHC-mediated biological output is very complicated. This review summarizes the pathophysiological relevance of 27-OHC in various tissues, with a special discussion on their functions in human diseases.

Copyright © 2021 Elsevier Ltd. All rights reserved.

Address: New Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, 41061, Republic of Korea.; Department of Life Science and Environmental Biochemistry, Life and Industry Convergence Research Institute, Pusan National University, Miryang, 50463, Republic of Korea.; Department of Convergence Medicine, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea.; Neurodegenerative Disease Research Group, Korea Brain Research Institute, Daegu, 41068, Republic of Korea; Department of Brain-Cognitive Science, Daegu-Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Republic of Korea.; Department of Physiology, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea. Electronic address: [email protected].; Neurodegenerative Disease Research Group, Korea Brain Research Institute, Daegu, 41068, Republic of Korea. Electronic address: [email protected].; Department of Convergence Medicine, Pusan National University School of Medicine, Yangsan, 50612, Republic of Korea. Electronic address: [email protected].

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