Skip to main content
. 2024 Jan 24;4(3):336–349. doi: 10.1038/s43587-023-00560-5

Extended Data Fig. 4. Effect of uPAR CAR T cells on aged tissues.

Extended Data Fig. 4

a-c, Quantification of SA-β-Gal–positive cells in adipose tissue, liver and pancreas 20 days after cell infusion (n = 3 for UT; n = 3 for h.19-m.28z; n = 4 for m.uPAR-m.28z). d-f, Quantification of uPAR-positive cells in adipose tissue, liver and pancreas 20 days after cell infusion (n = 3 per group). g-j, Percentage of dendritic cells and uPAR+ dendritic cells in the adipose tissue (g,h) or liver (i,j) 20 days after cell infusion (n = 3 for UT; n = 3 for h.19-m.28z; n = 4 for m.uPAR-m.28z). k-n, Percentage of macrophages and uPAR+ macrophages in the adipose tissue (k,l,) or liver (m,n) 20 days after cell infusion (n = 3 for UT; n = 3 for h.19-m.28z; n = 4 for m.uPAR-m.28z). o-r, Percentage of monocytes and uPAR+ monocytes in the adipose tissue (o,p) or liver (q,r) 20 days after cell infusion (n = 3 for UT; n = 3 for h.19-m.28z; n = 4 for m.uPAR-m.28z). Results of 1 independent experiment (a-r). Data are mean ± s.e.m.; p values from two-tailed unpaired Student’s t-test (a-r).

Source data