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©The Author(s) 2025.
World J Stem Cells. Jul 26, 2025; 17(7): 101929
Published online Jul 26, 2025. doi: 10.4252/wjsc.v17.i7.101929
Published online Jul 26, 2025. doi: 10.4252/wjsc.v17.i7.101929
Figure 1 X inactive-specific transcript overexpression enhanced mitochondrial function in neural stem cells.
A: Relative X inactive-specific transcript (XIST) expression level measured by PCR, indicating successful overexpression of XIST in neural stem cells; B: JC-1 staining assay showing the relative JC-1 intensity, reflecting mitochondrial membrane potential; C: Relative mitochondrial DNA copy number assessed by PCR, indicating an increase in mitochondrial biogenesis; D: Relative ATP production levels measured using an ATP assay kit, demonstrating enhanced ATP generation; E: Oxygen consumption rate result showed increased mitochondrial respiration in XIST-overexpressing neural stem cells. Data are presented as mean ± SD. aP < 0.01, bP < 0.001. XIST: X inactive-specific transcript; NC: Negative control; mtDNA: Mitochondrial DNA; OCR: Oxygen consumption rate; FCCP: Carbonyl cyanide 4-(trifluorome thoxy)phenylhydrazone.
- Citation: Zeng SX, Ye JT, Huang SH, Liu RX. X inactive-specific transcript regulates mitochondrial function and neuronal differentiation of stem cells via IGF2BP2/CPT1A axis in models of spinal cord injury. World J Stem Cells 2025; 17(7): 101929
- URL: https://www.wjgnet.com/1948-0210/full/v17/i7/101929.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v17.i7.101929