Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 6 | BMC Medicine

Fig. 6

From: Enhancing anti-CD3 mAb-mediated diabetes remission in autoimmune diabetes through regulation of dynamin-related protein 1(Drp1)-mediated mitochondrial dynamics in exhausted CD8+T-cell subpopulations

Fig. 6

Lrrk2 plays a role to alter the phosphorylation statu triggers mitochondrial fission (n = 3/group). A Sorted TPEX and TEX cells obtained from 16-week-old non-diabetic NOD mice were examined using qPCR to determine the expression of Dnm1l and Lrrk2. B Interaction network depicting between Dnm1l and Lrrk2 using the STRING database. C The Lrrk2 plasmid was used to transfect the 293 T cells. Cells were lysed for qPCR analyses. D The Lrrk2 plasmid was used to transfect the 293 T cells, followed by knockdown. Cells were lysed for qPCR analyses. E The 293 T cells were transfected with Lrrk2 plasmid or were transfected with Lrrk2 plasmid, followed by knockdown. Cells were lysed for immunoblotting analyses. F Western blot analysis was used to determine the protein expression in sorted TPEX and TEX cells that were separated from 8-week-old NY8.3 mice. G Sorted PD-1+CD8+ T cells in NY8.3 mice aged 6–8 weeks, stimulated them with anti-CD3 and anti-CD28 or IGRP206–214 for 3 days, with or without the Midiv-1. Collected the cells and analyzed using Western blotting. ***P < 0.001, ****P < 0.0001. Mann–Whitney test (A, C,D). Data represent two independent experiments

Back to article page