Journal Article

Collectin-11 promotes fibroblast proliferation and modulates their activation status and extracellular matrix synthesis

Zhang, Ting, Li, Gang, Li, Ke, Ma, Ning, Zhou, Wuding, Cao, Bo, Wang, Gang, Chen, Wan-Bing, Wu, Kun-Yi

2025

Overview

Collectin-11 (CL-11), a recently described soluble C-type lectin, has been shown to stimulate cell proliferation in fibroblasts and melanoma cells. However, its broader influence on fibroblast functions and the specific receptors mediating CL-11's effects remain to be elucidated. The EDU proliferation assay and WB detection of PCNA protein levels were used to evaluate the fibroblast proliferative effect after CL-11 stimulated. The qRT-PCR and WB detection of fibronectin and collagen I were used to evaluate the ECM production. The qRT-PCR detection of Il-6, Il-11, Tnfa, Il1b, Cxcl1, Egf, Tgfb1, Pdgfb were used to evaluate the cytokine production. The WB detection of ERK, AKT, STAT3, mTOR, SMAD2 and ACTIN were used to evaluate the activation of signaling pathway. The WB detection of ERK, AKT, STAT3, mTOR, SMAD2 and ACTIN were used to evaluate the activation of signaling pathway. The immunofluorescence and molecular docking experiments were used to detect the binding of CL-11 to EGFR/TGFRII. In this study, we demonstrate that CL-11 not only promotes fibroblast proliferation but also modulates their activation status and extracellular matrix (ECM) synthesis. Specifically, treatment with recombinant CL-11 (rCL-11) significantly upregulated the production of ECM proteins (fibronectin, collagen I), growth factors (EGF, TGF-β1), and proinflammatory cytokines/chemokines (IL-6, TNF-α, IL-11, IL-1β, CXCL1) in renal fibroblasts. Additionally, rCL-11 activated multiple intracellular signaling pathways, including ERK, AKT/mTOR, STAT3, and SMAD2. Further, EGFR and TGF-βRII were found to be abundantly expressed in renal fibroblasts, and molecular docking analysis along with immunofluorescence/confocal microscopy confirmed CL-11's interaction with these receptors. Our findings provide strong evidence that CL-11 plays a critical role in renal fibroblast proliferation and activation via engagement with EGFR and TGF-βRII, shedding light on the mechanisms by which CL-11 stimulates cellular activation and proliferation.

• Publisher: Frontiers Media SA,Frontiers Media S.A
• Subject: Actin / AKT protein / Antibodies / Biotechnology / Cell growth / Cell proliferation / Cell Proliferation - drug effects / Chemokines / Collagen (type I) / collectin-11 / Confocal microscopy / Cytokines - metabolism / EGFR and TGF-βRII / Epidermal growth factor / Epidermal growth factor receptors / ErbB Receptors - metabolism / Ethics / Extracellular matrix / Extracellular Matrix - metabolism / fibroblast function / Fibroblasts / Fibroblasts - metabolism / Fibronectin / Growth factors / Humans / Immunofluorescence / Immunology / Interleukin 11 / Interleukin 6 / Intracellular signalling / Ischemia / Kidneys / Melanoma / Molecular Docking Simulation / Morphology / PCNA protein / Penicillin / Polymerase chain reaction / Proteins / Receptor, Transforming Growth Factor-beta Type II - metabolism / renal fibroblast / Signal Transduction / Smad2 protein / Stat3 protein / TOR protein / Tumor necrosis factor-α