A human brain map of mitochondrial respiratory capacity and diversity, 2025, Mosharov et al.

Discussion in 'Other health news and research' started by SNT Gatchaman, Mar 27, 2025.

  1. SNT Gatchaman

    SNT Gatchaman Senior Member (Voting Rights) Staff Member

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    A human brain map of mitochondrial respiratory capacity and diversity
    Mosharov, Eugene V.; Rosenberg, Ayelet M.; Monzel, Anna S.; Osto, Corey A.; Stiles, Linsey; Rosoklija, Gorazd B.; Dwork, Andrew J.; Bindra, Snehal; Junker, Alex; Zhang, Ya; Fujita, Masashi; Mariani, Madeline B.; Bakalian, Mihran; Sulzer, David; De Jager, Philip L.; Menon, Vilas; Shirihai, Orian S.; Mann, J. John; Underwood, Mark D.; Boldrini, Maura; Thiebaut de Schotten, Michel; Picard, Martin

    Mitochondrial oxidative phosphorylation (OXPHOS) powers brain activity1,2 , and mitochondrial defects are linked to neurodegenerative and neuropsychiatric disorders3,4 . To understand the basis of brain activity and behaviour, there is a need to define the molecular energetic landscape of the brain5–10 .

    Here, to bridge the scale gap between cognitive neuroscience and cell biology, we developed a physical voxelization approach to partition a frozen human coronal hemisphere section into 703 voxels comparable to neuroimaging resolution (3 × 3 × 3 mm). In each cortical and subcortical brain voxel, we profiled mitochondrial phenotypes, including OXPHOS enzyme activities, mitochondrial DNA and volume density, and mitochondria-specific respiratory capacity.

    We show that the human brain contains diverse mitochondrial phenotypes driven by both topology and cell types. Compared with white matter, grey matter contains >50% more mitochondria. Moreover, the mitochondria in grey matter are biochemically optimized for energy transformation, particularly among recently evolved cortical brain regions. Scaling these data to the whole brain, we created a backwards linear regression model that integrates several neuroimaging modalities 11 to generate a brain-wide map of mitochondrial distribution and specialization. This model predicted mitochondrial characteristics in an independent brain region of the same donor brain.

    This approach and the resulting MitoBrainMap of mitochondrial phenotypes provide a foundation for exploring the molecular energetic landscape that enables normal brain function. This resource also relates to neuroimaging data and defines the subcellular basis for regionalized brain processes relevant to neuropsychiatric and neurodegenerative disorders. All data are available at http://humanmitobrainmap.bcblab.com.

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  2. Creekside

    Creekside Senior Member (Voting Rights)

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    Maybe that could explain the variations in ME symptoms. If ME does affect mitochondrial activity, it might not affect all these diverse phenotypes equally, and may or may not affect mitochondria outside the brain. One person might have severe reduction in ability to use muscles, while another doesn't, but has hearing hypersensitivity.
     

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