Table 1.
Fibrotic diseases | Target cell | Possible role in diseases | References |
---|---|---|---|
Liver fibrosis | Hepatic stellate cells | RhoA/ROCK1 signal pathways; inhibiting the expression of α-SMA, collagen-1, and TGF-β1 | (Chen et al., 2014; Ren et al. 2019) |
Pulmonary fibrosis | Alveolar type II cells | Reducing the levels of TNF-α and TGF-β1; decreasing alveolar type II cell apoptosis | (Nishimoto et al. 2015; Richter et al., 2009) |
Systemic sclerosis | Fibroblasts | Reducing levels of Egr-1, LOX | (Yamaguchi et al. 2012) |
Hypertrophic scar | Skin fibroblasts/hypertrophic scar fibroblasts (HSFs) | PDGFRβ/ERK pathway; inhibiting HSFs proliferation and inducing its apoptosis | (Gong et al. 2016; Gong et al. 2017; Li & Ren 2017) |
Arthritis | Synovial fibroblasts | Downregulating the level of cyclin-D1 and PCNA; inhibiting the NF-κB and MAPKs signaling pathways | (Chen et al. 2016; Huang et al. 2008; Huang et al. 2014) |
Myocardial remodeling | Myofibroblasts | Stimulating proliferation and migration of myofibroblasts | (Isobe et al., 2010; Sugiyama et al., 2018) |
ROCK1: Rho-associated kinase 1; α-SMA: α-smooth muscle actin; TNF-α: tumor necrosis factor α; TGF-β1: transforming growth factor β1; Egr-1: early growth response-1; LOX: lysyl oxidase; PDGFRβ: platelet-derived growth factor receptor β; ERK: extracellular signal-regulated kinase; PCNA: proliferating cell nuclear antigen; NF-κB: nuclear factor-κB; MAPK: mitogen-activated protein kinase.