(A) Representative Ly6G immunohistochemistry images from liver
sections. Scale bar=50 μm (n=8 mice/group and average of 3–5
images per mice). (B) Quantification of percentage area of Ly6G+
positive cells using Image J. Whole-cell liver lysates were used to detect
CXCL1(C), LCN2 (D), NE (G) and Cit-H3 (H) by ELISA. (n=3–8 mice/group).
(E-F) Levels of LCN2 and NE in serum as measured by ELISA
(n=3–5mice/group). (I-J) Co-immunofluorescence staining with NE and
Histone H3 (I) and with LCN2 and Histone H3 (J) to visualize NETs production in
mouse liver. scale bar=50 μm. Whole-cell human liver lysates were used to
detect CXCL1(K), LCN2 (L), and NE (M) by ELISA. (n=6 patients/MASH, n=5
patients/AH (BMI≤25) and n=7 patients/AH (BMI≥25)). *
p<0.05, **p<0.005, ***p<0.0005, ****p<0.0000