Steroidal triterpenes of cholesterol synthesis

Ačimovič, Jure (avtor), Rozman, Damjana (avtor)

Cholesterol synthesis is a ubiquitous and housekeeping metabolic pathway that leads to cholesterol, an essential structural component of mammalian cell membranes, required for proper membrane permeability and fluidity. The last part of the pathway involves steroidal triterpenes with cholestane ring structures. It starts by conversion of acyclic squalene into lanosterol, the first sterol intermediate of the pathway, followed by production of 20 structurally very similar steroidal triterpene molecules in over 11 complex enzyme reactions. Due to the structural similarities of sterol intermediates and the broad substrate specificity of the enzymes involved (especially sterol-Δ$^{24}$-reductase; DHCR24) the exact sequence of the reactions between lanosterol and cholesterol remains undefined. This article reviews all hitherto known structures of post-squalene steroidal triterpenes of cholesterol synthesis, their biological roles and the enzymes responsible for their synthesis. Furthermore, it summarises kinetic parameters of enzymes (V$_{max}$ and K$_m$) and sterol intermediate concentrations from various tissues. Due to the complexity of the post-squalene cholesterol synthesis pathway, future studies will require a comprehensive meta-analysis of the pathway to elucidate the exact reaction sequence in different tissues, physiological or disease conditions. A major reason for the standstill of detailed late cholesterol synthesis research was the lack of several steroidal triterpene standards. We aid to this efforts by summarizing commercial and laboratory standards, referring also to chemical syntheses of meiosis-activating sterols.

• Jezik: Angleški jezik
• Ključne besede: sterols, steroidal triterpenes, cholesterol synthesis, post-squalene pathway
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.02 - Pregledni znanstveni članek
• Organizacija: MF - Medicinska fakulteta
• Status publikacije: Objavljeno
• Različica publikacije: Objavljena publikacija
• Leto izida: 2013
• Št. strani: Str. 4002-4017
• Številčenje: Vol. 18, iss. 4
• PID: 20.500.12556/RUL-129498
• UDK: 577
• ISSN pri članku: 1420-3049
• DOI: 10.3390/molecules18044002
• COBISS.SI-ID: 30538457
• Datum objave v RUL: 02.09.2021

AČIMOVIČ, Jure in ROZMAN, Damjana, 2013, Steroidal triterpenes of cholesterol synthesis. Molecules [na spletu]. 2013. Vol. 18, no. 4, p. 4002–4017. [Dostopano 4 april 2025]. DOI 10.3390/molecules18044002. Pridobljeno s: https://repozitorij.uni-lj.si/IzpisGradiva.php?lang=slv&id=129498

Gradivo je del revije

• Naslov: Molecules
• Skrajšan naslov: Molecules
• Založnik: MDPI
• ISSN: 1420-3049
• COBISS.SI-ID: 18462981

Licence

• Licenca: CC BY 3.0, Creative Commons Priznanje avtorstva 3.0 Nedoločena
• Povezava: https://creativecommons.org/licenses/by/3.0/deed.sl
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• Začetek licenciranja: 04.04.2013

Sekundarni jezik

• Jezik: Slovenski jezik
• Ključne besede: steroli, steroidni triterpeni, sinteza holesterola

Projekti

• Financer: ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
• Številka projekta: P1-0104
• Naslov: Funkcijska genomika in biotehnologija za zdravje

• Financer: ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
• Številka projekta: J7-4053
• Naslov: Funkcijska genomika ravnovesja holesterola: vloga lanosterol 14alfa-demetilaze (CYP51) pri razvoju metaboličnih obolenj