Your browser doesn't support javascript.
loading
Quantitative Assessment of Morphological Changes in Lipid Droplets and Lipid-Mito Interactions with Aging in Brown Adipose.
Crabtree, Amber; Neikirk, Kit; Pinette, Julia; Whiteside, Aaron; Shao, Bryanna; McKenzie, Jessica; Vue, Zer; Vang, Larry; Le, Han; Dermici, Mert; Ahmad, Taseer; Owens, Trinity Celeste; Oliver, Ashton; Zeleke, Faben; Beasley, Heather K; Lopez, Edgar Garza; Scudese, Estevão; Rodman, Taylor; Kabugi, Kinuthia; Koh, Alice; Navarro, Suzanne; Lam, Jacob; Kirk, Ben; Mungai, Margaret; Sweetwyne, Mariya; Koh, Ho-Jin; Zaganjor, Elma; Damo, Steven M; Gaddy, Jennifer A; Kirabo, Annet; Murray, Sandra A; Cooper, Anthonya; Williams, Clintoria; McReynolds, Melanie R; Marshall, Andrea G; Hinton, Antentor.
Afiliação
  • Crabtree A; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Neikirk K; The Frist Center for Autism and Innovation, Vanderbilt University, Nashville, TN, 37212, USA.
  • Pinette J; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Whiteside A; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Shao B; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • McKenzie J; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Vue Z; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Vang L; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Le H; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Dermici M; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Ahmad T; Department of Medicine, Division Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Owens TC; Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Oliver A; Department of Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Punjab,40100, Pakistan.
  • Zeleke F; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Beasley HK; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Lopez EG; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Scudese E; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Rodman T; Department of Internal Medicine, University of Iowa, Iowa City, IA, 52242, USA.
  • Kabugi K; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Koh A; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Navarro S; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Lam J; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Kirk B; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Mungai M; Department of Internal Medicine, University of Iowa, Iowa City, IA, 52242, USA.
  • Sweetwyne M; Department of Internal Medicine, University of Iowa, Iowa City, IA, 52242, USA.
  • Koh HJ; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Zaganjor E; Department of Internal Medicine, University of Iowa, Iowa City, IA, 52242, USA.
  • Damo SM; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195, USA.
  • Gaddy JA; Department of Biological Sciences, Tennessee State University, Nashville, TN 37209, USA.
  • Kirabo A; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.
  • Murray SA; Department of Life and Physical Sciences, Fisk University, Nashville, TN, 37208, USA.
  • Cooper A; Division of Infectious Diseases, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA; Tennessee Valley Healthcare Systems, U.S. Department of Veterans Affairs, Nashville, TN, 37212, USA.
  • Williams C; Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.
  • McReynolds MR; Department of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Marshall AG; Department of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
  • Hinton A; Department of Neuroscience, Cell Biology and Physiology, Wright State University, Dayton, OH 45435 USA.
bioRxiv ; 2024 May 21.
Article em En | MEDLINE | ID: mdl-38826465
ABSTRACT
The physical characteristics of brown adipose tissue (BAT) are defined by the presence of multilocular lipid droplets (LD) within the brown adipocytes and a high abundance of iron-containing mitochondria, which give it its characteristic color. Normal mitochondrial function is, in part, regulated by organelle-to-organelle contacts. Particularly, the contact sites that mediate mitochondria-LD interactions are thought to have various physiological roles, such as the synthesis and metabolism of lipids. Aging is associated with mitochondrial dysfunction, and previous studies show that there are changes in mitochondrial structure and proteins that modulate organelle contact sites. However, how mitochondria-LD interactions change with aging has yet to be fully clarified. Therefore, we sought to define age-related changes in LD morphology and mitochondria-lipid interactions in BAT. We examined the three-dimensional morphology of mitochondria and LDs in young (3-month) and aged (2-year) murine BAT using serial block face-scanning electron microscopy and the Amira program for segmentation, analysis, and quantification. Analysis showed reductions in LD volume, area, and perimeter in aged samples compared to young samples. Additionally, we observed changes in LD appearance and type in aged samples compared to young samples. Notably, we found differences in mitochondrial interactions with LDs, which could implicate that these contacts may be important for energetics in aging. Upon further investigation, we also found changes in mitochondrial and cristae structure for mitochondria interacting with LD lipids. Overall, these data define the nature of LD morphology and organelle-organelle contacts during aging and provide insight into LD contact site changes that interconnect biogerontology and mitochondrial functionality, metabolism, and bioactivity in aged BAT.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos