2D). Regeneration ratios were calculated to estimate the amount of liver regeneration over time. We observed a significant difference in the regeneration ratio (resected/regenerated weight) on days 3-5 in CO-treated mice versus control (Fig. 2E). Additionally, we

calculated a ratio of the number of pH3-positive cells to gram of regenerated tissue and also observed a significant difference between CO and air on day 3 (43.65 versus 35.9 positive cells/g tissue, P < 0.03 air versus CO). Taken together, these data demonstrate that CO accelerates liver regeneration and, importantly, imparts significant beneficial effects on the overall health status of the mice after PHTx as evidenced by body weight recovery and maintenance of primary liver function. After PHTx, numerous growth factors play important roles in regeneration of liver tissue, most notably of which is HGF, Talazoparib mouse which is generated and released primarily from the stellate cell.26 HGF was measured by enzyme-linked immunosorbent assay (ELISA) in liver tissue lysates, which increased over baseline after PHTx in both air and CO-treated mice. CO-treated mice, however, showed peak HGF expression as early as

12 hours after PHTx, whereas air controls did not peak until 24 hours (Fig. 3A). The staining pattern of HGF revealed that HGF was not released from Vadimezan price hepatocytes, but produced by stellate

cells, corroborated by specific colocalization with desmin, a specific stellate cell marker with no colocalization with F4.80 positive Kupffer cells (Fig. 3B-E).27 transforming Hydroxychloroquine growth factor beta (TGF-β) and interleukin-6 (IL-6) are also increased in response to partial hepatectomy.29, 30 Both were elevated after resection and we observed no difference between air and CO-treated mice over time (Fig. 3F,G). These findings suggest that CO accelerates liver regeneration in large part by more rapid and enhanced stellate cell-derived HGF expression and not by way of TGF-β and IL-6 expression. Hepatocyte cell size increases significantly after PHTx, which is thought to be due to the induction of prosurvival signaling and increased protein synthesis as the cells ready for regeneration.31 Based on the effects we observed on HGF expression and PT-INR, we next tested whether CO influenced the relative size of hepatocytes. Hepatocyte size was unchanged in air-treated, PHTx mice 24 hours after hepatectomy and increased nearly 2-fold 48 hours after PHTx compared to naive nonhepatectomized livers (Fig. 4A). The change in size correlated with the peak in proliferative index (Fig. 1). In contrast, CO-treated mice showed a more rapid increase (1.4-fold) in cell size at 24 hours versus air-treated controls (Fig. 4A), again corroborating the proliferation data shown in Fig. 1.