Single‐Cell RNA and Transcriptome Sequencing to Analyze the Role of Lactate Metabolism in Traumatic Brain Injury Astrocytes DOI Creative Commons

Bu Zhang,

Yuqian Zhou, Feng Xu

и другие.

Brain and Behavior, Год журнала: 2025, Номер 15(5)

Опубликована: Май 1, 2025

ABSTRACT Purpose After traumatic brain injury (TBI), ischemia and hypoxia of tissue, glucose undergoes anaerobic fermentation, leading to a large accumulation lactic acid. Our aim was explore the role lactate metabolism in cells after TBI. Method In scRNA‐seq dataset, 10‐week‐old male C57BL/6 J mice were randomized undergo mild fluid percussion or sham surgery, we analyzed frontal cortex tissue during acute (24 h) subacute (7 days) phases TBI at single‐cell resolution. Cell cycle evaluated, principal component analysis performed. populations identified visualized using UMAP downscaling technique. Differentially expressed genes (DEGs) “FindAllMarkers” algorithm. addition, set related evaluated AUCell score. GO KEGG enrichment analyses performed investigate functional pathways DEGs astrocytes Results A total 13 cell distinguished, including neurons, astrocytes, oligodendrocyte progenitors. The number endothelial reduced group compared with group. During phase TBI, enhanced interactions between brain‐associated cells, especially precursor observed. Several signaling pathways, EGF, CSF, MIF inflammatory factors as well PSAP PTN neurotrophic factor significantly Lactate scores elevated group, astrocytes. phase, frequency intercellular communication increased but its intensity decreased. Astrocytes remained high levels both phases. closely associated Subsequently, NADH:ubiquinone oxidoreductase subunit B9 ( Ndufb9 ) cytochrome c oxidase 8A Cox8a key players showed consistent upward trend following transcriptomic data. Conclusion play an important These findings provide new insights into cellular molecular mechanisms

Язык: Английский

Human umbilical cord mesenchymal stem cell-derived exosomes provide neuroprotection in traumatic brain injury through the lncRNA TUBB6/Nrf2 pathway DOI
Li Zhang,

Wanshan Bai,

Yaonan Peng

и другие.

Brain Research, Год журнала: 2023, Номер 1824, С. 148689 - 148689

Опубликована: Ноя. 27, 2023

Язык: Английский

Процитировано

13

Reprogramming metabolic microenvironment for nerve regeneration via waterborne polylactic acid-polyurethane copolymer scaffolds DOI
Yuan Feng, Jinlin Chen, Xiao Wang

и другие.

Biomaterials, Год журнала: 2024, Номер 315, С. 122942 - 122942

Опубликована: Ноя. 1, 2024

Язык: Английский

Процитировано

5

Research Advances in Neuroblast Migration in Traumatic Brain Injury DOI Creative Commons
Na Wu,

Wenlang Li,

Qiang Chen

и другие.

Molecular Neurobiology, Год журнала: 2024, Номер 61(10), С. 1 - 13

Опубликована: Март 20, 2024

Neuroblasts were first derived from the adult mammalian brains in 1990s by Reynolds et al. Since then, persistent neurogenesis subgranular zone (SGZ) of hippocampus and subventricular (SVZ) has gradually been recognized. To date, reviews on neuroblast migration have largely investigated glial cells molecular signaling mechanisms, while relationship between vasculature cell remains a mystery. Thus, this paper underlines partial biological features unravels significance mechanisms process to further clarify theoretically neural repair mechanism after brain injury. Neuroblast presents three modes according characteristics that act as scaffolds during process: gliophilic migration, neurophilic vasophilic migration. Many molecules, including brain-derived neurotrophic factor (BDNF), stromal cell-derived 1 (SDF-1), vascular endothelial growth (VEGF), angiopoietin-1 (Ang-1), affect synergistically regulating neuroblasts target areas along blood vessels. However, precise role vessels needs be explored. The in-depth study will most probably provide theoretical basis breakthrough for clinical treatment injury diseases.

Язык: Английский

Процитировано

4

Sphingolipid changes in mouse brain and plasma after mild traumatic brain injury at the acute phases DOI Creative Commons
Koushik Mondal,

Nobel A. Del Mar,

Ashlyn A. Gary

и другие.

Lipids in Health and Disease, Год журнала: 2024, Номер 23(1)

Опубликована: Июнь 27, 2024

Traumatic brain injury (TBI) causes neuroinflammation and can lead to long-term neurological dysfunction, even in cases of mild TBI (mTBI). Despite the substantial burden this disease, management is precluded by an incomplete understanding its cellular mechanisms. Sphingolipids (SPL) their metabolites have emerged as key orchestrators biological processes related tissue injury, neuroinflammation, inflammation resolution. No study so far has investigated comprehensive sphingolipid profile changes immediately following animal models or human cases. In study, metabolite composition was examined during acute phases plasma mice mTBI.

Язык: Английский

Процитировано

4

Single‐Cell RNA and Transcriptome Sequencing to Analyze the Role of Lactate Metabolism in Traumatic Brain Injury Astrocytes DOI Creative Commons

Bu Zhang,

Yuqian Zhou, Feng Xu

и другие.

Brain and Behavior, Год журнала: 2025, Номер 15(5)

Опубликована: Май 1, 2025

ABSTRACT Purpose After traumatic brain injury (TBI), ischemia and hypoxia of tissue, glucose undergoes anaerobic fermentation, leading to a large accumulation lactic acid. Our aim was explore the role lactate metabolism in cells after TBI. Method In scRNA‐seq dataset, 10‐week‐old male C57BL/6 J mice were randomized undergo mild fluid percussion or sham surgery, we analyzed frontal cortex tissue during acute (24 h) subacute (7 days) phases TBI at single‐cell resolution. Cell cycle evaluated, principal component analysis performed. populations identified visualized using UMAP downscaling technique. Differentially expressed genes (DEGs) “FindAllMarkers” algorithm. addition, set related evaluated AUCell score. GO KEGG enrichment analyses performed investigate functional pathways DEGs astrocytes Results A total 13 cell distinguished, including neurons, astrocytes, oligodendrocyte progenitors. The number endothelial reduced group compared with group. During phase TBI, enhanced interactions between brain‐associated cells, especially precursor observed. Several signaling pathways, EGF, CSF, MIF inflammatory factors as well PSAP PTN neurotrophic factor significantly Lactate scores elevated group, astrocytes. phase, frequency intercellular communication increased but its intensity decreased. Astrocytes remained high levels both phases. closely associated Subsequently, NADH:ubiquinone oxidoreductase subunit B9 ( Ndufb9 ) cytochrome c oxidase 8A Cox8a key players showed consistent upward trend following transcriptomic data. Conclusion play an important These findings provide new insights into cellular molecular mechanisms

Язык: Английский

Процитировано

0