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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Zhe Sun (328682) (author)
مؤلفون آخرون: Zicheng Ma (14071216) (author), Wandi Cao (20553288) (author), Chenlong Jiang (14071219) (author), Lei Guo (36221) (author), Kesen Liu (9086343) (author), Yanni Gao (6250973) (author), Juan Bai (798838) (author), Jiang Pi (817619) (author), Ping Jiang (243020) (author), Xing Liu (221084) (author)
منشور في: 2025
الموضوعات:
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الوصف
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>