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- Ackerman, Jacobo Miranda1
- Alvarez-Jarreta, Jorge1
- Arya, Arvind1
- Bentley, Kirsten1
- Brosch, Mario1
- Brown, Richard William1
- Buch, Stephan1
- Buurma, Niklaas J1
- Chandrasekaran, Preethi1
- Choi, Yujeong1
- Coskun, Ünal1
- Dane, Adriaan D1
- Fu, Xiaorong1
- Geley, Stephan1
- Golderer, Georg1
- Griffiths, William J1
- Gross, Justus1
- Hampe, Jochen1
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- Has, Canan1
- Heyman, James1
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- Jenkins, P Vince1
- Jeong, Mi Gyeong1
- Keller, Markus A1
Regular Research Articles
5 Results
- Research ArticleOpen Access
Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdown
Journal of Lipid ResearchVol. 63Issue 6100222Published online: May 7, 2022- Sabrina Sailer
- Katharina Lackner
- Mia L. Pras-Raves
- Eric J.M. Wever
- Jan B. van Klinken
- Adriaan D. Dane
- and others
Cited in Scopus: 0Little is known about the physiological role of alkylglycerol monooxygenase (AGMO), the only enzyme capable of cleaving the 1-O-alkyl ether bond of ether lipids. Expression and enzymatic activity of this enzyme can be detected in a variety of tissues including adipose tissue. This labile lipolytic membrane-bound protein uses tetrahydrobiopterin as a cofactor, and mice with reduced tetrahydrobiopterin levels have alterations in body fat distribution and blood lipid concentrations. In addition, manipulation of AGMO in macrophages led to significant changes in the cellular lipidome, and alkylglycerolipids, the preferred substrates of AGMO, were shown to accumulate in mature adipocytes. - Research ArticleOpen Access
The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses
Journal of Lipid ResearchVol. 63Issue 6100208Published online: April 14, 2022- Zack Saud
- Victoria J. Tyrrell
- Andreas Zaragkoulias
- Majd B. Protty
- Evelina Statkute
- Anzelika Rubina
- and others
Cited in Scopus: 9The lipid envelope of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an essential component of the virus; however, its molecular composition is undetermined. Addressing this knowledge gap could support the design of antiviral agents as well as further our understanding of viral-host protein interactions, infectivity, pathogenicity, and innate immune system clearance. Lipidomics revealed that the virus envelope comprised mainly phospholipids (PLs), with some cholesterol and sphingolipids, and with cholesterol/phospholipid ratio similar to lysosomes. - Research ArticleOpen Access
Nonalcoholic fatty liver disease stratification by liver lipidomics
Journal of Lipid ResearchVol. 62100104Published online: August 9, 2021- Olga Vvedenskaya
- Tim Daniel Rose
- Oskar Knittelfelder
- Alessandra Palladini
- Judith Andrea Heidrun Wodke
- Kai Schuhmann
- and others
Cited in Scopus: 18Nonalcoholic fatty liver disease (NAFLD) is a common metabolic dysfunction leading to hepatic steatosis. However, NAFLD's global impact on the liver lipidome is poorly understood. Using high-resolution shotgun mass spectrometry, we quantified the molar abundance of 316 species from 22 major lipid classes in liver biopsies of 365 patients, including nonsteatotic patients with normal or excessive weight, patients diagnosed with NAFL (nonalcoholic fatty liver) or NASH (nonalcoholic steatohepatitis), and patients bearing common mutations of NAFLD-related protein factors. - Research ArticleOpen Access
Amodiaquine promotes testosterone production and de novo synthesis of cholesterol and triglycerides in Leydig cells
Journal of Lipid ResearchVol. 62100152Published online: November 18, 2021- Yujeong Choi
- Eun Goo Lee
- Gibbeum Lee
- Mi Gyeong Jeong
- Hyo Kyeong Kim
- Ji-Hyun Oh
- and others
Cited in Scopus: 0Testosterone is a hormone essential for male reproductive function. It is produced primarily by Leydig cells in the testicle through activation of steroidogenic acute regulatory protein and a series of steroidogenic enzymes, including a cytochrome P450 side-chain cleavage enzyme (cytochome P450 family 11 subfamily A member 1), 17α-hydroxylase (cytochrome P450 family 17 subfamily A member 1), and 3β-hydroxysteroid dehydrogenase. These steroidogenic enzymes are mainly regulated at the transcriptional level, and their expression is increased by the nuclear receptor 4A1. - Research ArticleOpen Access
Hepatic deletion of Mboat7 (LPIAT1) causes activation of SREBP-1c and fatty liver
Journal of Lipid ResearchVol. 62100031Published online: February 5, 2021- Mingfeng Xia
- Preethi Chandrasekaran
- Shunxing Rong
- Xiaorong Fu
- Matthew A. Mitsche
Cited in Scopus: 0Genetic variants that increase the risk of fatty liver disease and cirrhosis have recently been identified in the proximity of membrane-bound O-acyltransferase domain-containing 7 (MBOAT7). To elucidate the link between these variants and fatty liver disease, we characterized Mboat7 liver-specific KO mice (Mboat7 LSKO). Chow-fed Mboat7 LSKO mice developed fatty livers and associated liver injury. Lipidomic analysis of liver using MS revealed a pronounced reduction in 20-carbon PUFA content in phosphatidylinositols (PIs) but not in other phospholipids.