Frontiers in Physiology (Apr 2024)
The nonvesicular sterol transporter Aster-C plays a minor role in whole body cholesterol balance
- Rakhee Banerjee,
- Rakhee Banerjee,
- Rachel C. Hohe,
- Rachel C. Hohe,
- Shijie Cao,
- Shijie Cao,
- Bryan M. Jung,
- Bryan M. Jung,
- Anthony J. Horak,
- Iyappan Ramachandiran,
- Iyappan Ramachandiran,
- William J. Massey,
- William J. Massey,
- William J. Massey,
- Venkateshwari Varadharajan,
- Venkateshwari Varadharajan,
- Natalie I. Zajczenko,
- Natalie I. Zajczenko,
- Amy C. Burrows,
- Amy C. Burrows,
- Sumita Dutta,
- Sumita Dutta,
- Maryam Goudarzi,
- Maryam Goudarzi,
- Kala Mahen,
- Kala Mahen,
- Abigail Carter,
- Robert N. Helsley,
- Robert N. Helsley,
- Scott M. Gordon,
- Richard E. Morton,
- Christopher Strauch,
- Belinda Willard,
- Camelia Baleanu Gogonea,
- Valentin Gogonea,
- Matteo Pedrelli,
- Paolo Parini,
- J. Mark Brown,
- J. Mark Brown
Affiliations
- Rakhee Banerjee
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Rakhee Banerjee
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Rachel C. Hohe
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Rachel C. Hohe
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Shijie Cao
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Shijie Cao
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Bryan M. Jung
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Bryan M. Jung
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Anthony J. Horak
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Iyappan Ramachandiran
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Iyappan Ramachandiran
- Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH, United States
- William J. Massey
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- William J. Massey
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- William J. Massey
- Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Venkateshwari Varadharajan
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Venkateshwari Varadharajan
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Natalie I. Zajczenko
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Natalie I. Zajczenko
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Amy C. Burrows
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Amy C. Burrows
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Sumita Dutta
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Sumita Dutta
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Maryam Goudarzi
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Maryam Goudarzi
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Kala Mahen
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- Kala Mahen
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Abigail Carter
- Department of Physiology and the Saha Cardiovascular Research Center, University of Kentucky College of Medicine, Lexington, KY, United States
- Robert N. Helsley
- Department of Physiology and the Saha Cardiovascular Research Center, University of Kentucky College of Medicine, Lexington, KY, United States
- Robert N. Helsley
- Department of Internal Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Kentucky College of Medicine, Lexington, KY, United States
- Scott M. Gordon
- Department of Physiology and the Saha Cardiovascular Research Center, University of Kentucky College of Medicine, Lexington, KY, United States
- Richard E. Morton
- Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH, United States
- Christopher Strauch
- Proteomics and Metabolomics Core, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Belinda Willard
- Proteomics and Metabolomics Core, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- Camelia Baleanu Gogonea
- Department of Chemistry, Cleveland State University, Cleveland, OH, United States
- Valentin Gogonea
- Department of Chemistry, Cleveland State University, Cleveland, OH, United States
- Matteo Pedrelli
- Department of Laboratory Medicine, Karolinska Institute, Huddinge, Sweden
- Paolo Parini
- Department of Laboratory Medicine, Karolinska Institute, Huddinge, Sweden
- J. Mark Brown
- Department of Cancer Biology, Lerner Research Institute of the Cleveland Clinic, Cleveland, OH, United States
- J. Mark Brown
- Center for Microbiome and Human Health, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States
- DOI
- https://doi.org/10.3389/fphys.2024.1371096
- Journal volume & issue
-
Vol. 15
Abstract
Introduction:The Aster-C protein (encoded by the Gramd1c gene) is an endoplasmic reticulum (ER) resident protein that has been reported to transport cholesterol from the plasma membrane to the ER. Although there is a clear role for the closely-related Aster-B protein in cholesterol transport and downstream esterification in the adrenal gland, the specific role for Aster-C in cholesterol homeostasis is not well understood. Here, we have examined whole body cholesterol balance in mice globally lacking Aster-C under low or high dietary cholesterol conditions.Method:Age-matched Gramd1c+/+ and Gramd1c−/− mice were fed either low (0.02%, wt/wt) or high (0.2%, wt/wt) dietarycholesterol and levels of sterol-derived metabolites were assessed in the feces, liver, and plasma.Results:Compared to wild type controls (Gramd1c+/+) mice, mice lackingGramd1c (Gramd1c−/−) have no significant alterations in fecal, liver, or plasma cholesterol. Given the potential role for Aster C in modulating cholesterol metabolism in diverse tissues, we quantified levels of cholesterol metabolites such as bile acids, oxysterols, and steroid hormones. Compared to Gramd1c+/+ controls, Gramd1c−/− mice had modestly reduced levels of select bile acid species and elevated cortisol levels, only under low dietary cholesterol conditions. However, the vast majority of bile acids, oxysterols, and steroid hormones were unaltered in Gramd1c−/− mice. Bulk RNA sequencing in the liver showed that Gramd1c−/− mice did not exhibit alterations in sterol-sensitive genes, but instead showed altered expression of genes in major urinary protein and cytochrome P450 (CYP) families only under low dietary cholesterol conditions.Discussion:Collectively, these data indicate nominal effects of Aster-C on whole body cholesterol transport and metabolism under divergent dietary cholesterol conditions. These results strongly suggest that Aster-C alone is not sufficient to control whole body cholesterol balance, but can modestly impact circulating cortisol and bile acid levels when dietary cholesterol is limited.
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