Goat CCL5 promotes cell viability and inflammatory factors production in lung fibroblasts and macrophages

Comp Biochem Physiol C Toxicol Pharmacol. 2022 Sep:259:109389. doi: 10.1016/j.cbpc.2022.109389. Epub 2022 Jun 1.

Abstract

Inflammatory chemokine CCL5 can mediate the occurrence of inflammatory reactions and participate in various disease processes. (Ch)CCL5 gene of Jintang black goat (Capra hircus, C. hircus) was cloned. The CDS (coding sequences) was 276 bp in length and encoded 91 amino acids. The 26.5 kDa recombinant protein was expressed by Escherichia coli system and purified by Ni-Agarose. The viabilities of primary goat lung fibroblasts could be enhanced after treating with ChCCL5 protein (12.5, 25, 50 μg/mL) (P < 0.05). The expression levels of interleukin-1beta (IL-1β), interleukin 6 (IL-6), tumor necrosis factor (TNF-α), C-C motif chemokine ligand 2 (CCL2) and heat-shock proteins (Hsp70) genes were upregulated after treating with ChCCL5 protein (12.5, 25, 50 μg/mL). Besides, the viabilities and phagocytic abilities of primary mouse peritoneal macrophages could be enhanced after treating with ChCCL5 protein (12.5, 25, 50 μg/mL) (P < 0.05). The expression levels of IL-1β, IL-6, toll-like receptor 4 (TLR4), inducible nitric oxide synthase (iNOs) and TNF-α genes were upregulated after treating with ChCCL5 protein (12.5, 25, 50 μg/mL) (P < 0.05). These results indicated that goat CCL5 might play a role in the inflammatory response by regulating the inflammatory cytokines produced by lung fibroblasts and macrophages.

Keywords: CCL5; Cell viability; Inflammatory factors; Jintang black goat; Prokaryotic expression.

MeSH terms

  • Animals
  • Cell Survival
  • Chemokine CCL5* / metabolism
  • Fibroblasts* / metabolism
  • Goats / metabolism
  • Interleukin-6 / metabolism
  • Lung / metabolism
  • Macrophages* / metabolism
  • Mice
  • Nitric Oxide Synthase Type II / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Chemokine CCL5
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide Synthase Type II