Journal: Hepatobiliary Surgery and Nutrition
Article Title: EREG-secreting THBS1 + tissue monocytes are recruited by C5a to promote rapid liver regeneration in patients and mice during the ALPPS procedure
doi: 10.21037/hbsn-24-391
Figure Lengend Snippet: Proliferation phenotype of THBS1 + tissue monocytes. (A) t-SNE plot of the distribution of the Mo/Mφ population at ALPPS stage II. Results are color-coded according to the growth factor gene expression level. MP, Mo/Mφ population. (B) Violin and t-SNE plots of the EREG expression in THBS1 + tissue monocytes, i.e., THBS1 + tissue monocytes. (C) Network of hepatocyte receptor interactions (left panel) and bubble plot of monocyte cluster ligand and hepatocyte receptor interactions (right panel). (D) Bubble plot showing the expression of receptors in monocyte clusters. (E) Boxplot representing a comparison of the peak concentrations of EREG in the plasma of patients at ALPPS stages I and II. *, P<0.05. (F) Line chart showing the OD450 values of hepatocytes in the EREG group and control group following CCK-8 incubation. (G) In the liver tissue from the murine model of ALPPS, regeneration was impaired after systemic neutralization of EREG. (H) Survival analysis of EREG rescue versus vehicle treatment for mice with PHLF. *, P<0.05; **, P<0.01; ***, P<0.001 (actual P values were reported in results). ALPPS, associating liver partition and portal vein ligation for staged hepatectomy; CCK-8, Cell Counting Kit-8; EREG, epiregulin; FLR, future liver remnant; Mo, monocytes; Mφ, macrophages; MP, Mo/Mφ population; PHLF, post-hepatectomy liver failure; TM, tissue monocyte; t-SNE, t-distributed stochastic neighbor embedding.
Article Snippet: The cells were resuspended in minimum essential medium (MEM) containing 10% FBS with recombinant EREG (5 μg/mL; rmEpiregulin/CF, 1068-EP-050/CF, R&D Systems), recombinant AREG (5 μg/mL; rmAmphiregulin/CF, 989-AR-100/CF, R&D Systems), recombinant EREG plus recombinant AREG (5 μg/mL), or vehicle control and inoculated into a 96 well plate with 1,000 cells per well.
Techniques: Gene Expression, Expressing, Comparison, Clinical Proteomics, Control, CCK-8 Assay, Incubation, Neutralization, Ligation, Cell Counting