TY - JOUR
T1 - Quantitative assessment of morphological changes in lipid droplets and lipid–mito interactions with aging in brown adipose
AU - Crabtree, Amber
AU - Neikirk, Kit
AU - Pinette, Julia A.
AU - Whiteside, Aaron
AU - Shao, Bryanna
AU - Bedenbaugh, Jessica
AU - Vue, Zer
AU - Vang, Larry
AU - Le, Han
AU - Demirci, Mert
AU - Ahmad, Taseer
AU - Owens, Trinity Celeste
AU - Oliver, Ashton
AU - Zeleke, Faben
AU - Beasley, Heather K.
AU - Lopez, Edgar Garza
AU - Scudese, Estevão
AU - Rodman, Taylor
AU - Kabugi, Kinuthia
AU - Koh, Alice
AU - Navarro, Suzanne
AU - Lam, Jacob
AU - Kirk, Ben
AU - Mungai, Margaret
AU - Sweetwyne, Mariya
AU - Koh, Ho Jin
AU - Zaganjor, Elma
AU - Damo, Steven M.
AU - Gaddy, Jennifer A.
AU - Kirabo, Annet
AU - Murray, Sandra A.
AU - Cooper, Anthonya
AU - Williams, Clintoria
AU - McReynolds, Melanie R.
AU - Marshall, Andrea G.
AU - Hinton, Antentor
N1 - Publisher Copyright:
© 2024 The Author(s). Journal of Cellular Physiology published by Wiley Periodicals LLC.
PY - 2024/9
Y1 - 2024/9
N2 - The physical characteristics of brown adipose tissue (BAT) are defined by the presence of multilocular lipid droplets (LDs) 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. For example, 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 the 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. Our analyses showed reductions in LD volume, area, and perimeter in aged samples in comparison 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 the mitochondria interacting with LDs. 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 with mitochondrial function, metabolism, and bioactivity in aged BAT.
AB - The physical characteristics of brown adipose tissue (BAT) are defined by the presence of multilocular lipid droplets (LDs) 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. For example, 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 the 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. Our analyses showed reductions in LD volume, area, and perimeter in aged samples in comparison 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 the mitochondria interacting with LDs. 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 with mitochondrial function, metabolism, and bioactivity in aged BAT.
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U2 - 10.1002/jcp.31340
DO - 10.1002/jcp.31340
M3 - Article
C2 - 39138923
AN - SCOPUS:85201093846
SN - 0021-9541
VL - 239
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 9
M1 - e31340
ER -