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• W4313367629 endingPage "102229" @default.
• W4313367629 startingPage "102229" @default.
• W4313367629 abstract "Rab7 belongs to the Ras small GTPase superfamily, and abnormal expression of Rab7 can cause neuropathy and lipid metabolism diseases. Studies have shown that Rab7 plays a crucial role in the inner membrane translocase. However, the role of Rab7 in the regulatory mechanisms of cell survival in spinal cord injury remains unknown. We used a rat spinal cord injury (SCI) model to explore the cellular localization and expression of Rab7 after SCI in this study. Western blot analysis showed that Rab7 was expressed in the spinal cord tissue. On the first day, it significantly increased and peaked after SCI on the third day. Furthermore, western blotting also demonstrated that pyroptosis-related protein Gasdermin D (GSDMD), Caspase-1, apoptosis-associated speck-like protein (ASC) expression peaked after the third-day post-injury. Importantly, the immunohistochemistry analysis revealed that Rab7 was completely colocalized with ASC in neurons after SCI. These results suggested that Rab7 was colocalized with NeuN and ASC, involved in the pyroptosis of neurons, and closely related to the spinal cord after injury." @default.
• W4313367629 created "2023-01-06" @default.
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• W4313367629 date "2023-03-01" @default.
• W4313367629 modified "2023-10-16" @default.
• W4313367629 title "Upregulation of RAB7 is related to neuronal pyroptosis after spinal cord injury in rats" @default.
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• W4313367629 doi "https://doi.org/10.1016/j.jchemneu.2022.102229" @default.
• W4313367629 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36592695" @default.
• W4313367629 hasPublicationYear "2023" @default.
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