VDAC1-MCU channels mediate mitochondrial Ca<sup>2+</sup> entry and mitochondrial fission.
<p>(A-H) Marc-145 cells were infected with PRRSV (MOI = 0.1) for 24 h with or without VBIT-12 (A-D) or MCU-i4 (E-H) treatment. (A and E) Ca<sup>2+</sup> was detected by flow cytometry after Rhod-2 staining. (B and F) The cells were analyzed by confocal microscopy after staining wit...
محفوظ في:
| المؤلف الرئيسي: | |
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| مؤلفون آخرون: | , , , , , , , , , |
| منشور في: |
2025
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| الموضوعات: | |
| الوسوم: |
إضافة وسم
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| الملخص: | <p>(A-H) Marc-145 cells were infected with PRRSV (MOI = 0.1) for 24 h with or without VBIT-12 (A-D) or MCU-i4 (E-H) treatment. (A and E) Ca<sup>2+</sup> was detected by flow cytometry after Rhod-2 staining. (B and F) The cells were analyzed by confocal microscopy after staining with MitoTracker Red, PRRSV-N antibody and DAPI. The mitochondrial length was quantified from 25 cells per group (right panel). (C and G) The cell lysates were harvested for western blot analysis with antibodies against p-DRP1(S637), p-DRP1(S616), DRP1, PRRSV-N and β-actin. The levels of phosphorylated DRP1 were normalized to the total DRP1 protein, while the levels of other proteins were normalized to β-actin. (D and H) Quantification of the TCID<sub>50</sub> of PRRSV in cell supernatants. Data are expressed as means ± SD, n = 3 in A, D, E and H or n = 25 in B and F. *p<0.05; **p < 0.01; ***p < 0.001. The data are representative of results from three independent experiments.</p> |
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