Fish Collagen Peptides Protect against Cisplatin-Induced Cytotoxicity and Oxidative Injury by Inhibiting MAPK Signaling Pathways in Mouse Thymic Epithelial Cells.
Won Hoon SongHye-Yoon KimYe Seon LimSeon Yeong HwangChangyong LeeDo Young LeeYuseok MoonYong Jung SongSik YoonPublished in: Marine drugs (2022)
Thymic epithelial cells (TECs) account for the most abundant and dominant stromal component of the thymus, where T cells mature. Oxidative- or cytotoxic-stress associated injury in TECs, a significant and common problem in many clinical settings, may cause a compromised thymopoietic capacity of TECs, resulting in clinically significant immune deficiency disorders or impairment in the adaptive immune response in the body. The present study demonstrated that fish collagen peptides (FCP) increase cell viability, reduce intracellular levels of reactive oxygen species (ROS), and impede apoptosis by repressing the expression of Bax and Bad and the release of cytochrome c, and by upregulating the expression of Bcl-2 and Bcl-xL in cisplatin-treated TECs. These inhibitory effects of FCP on TEC damage occur via the suppression of ROS generation and MAPK (p38 MAPK, JNK, and ERK) activity. Taken together, our data suggest that FCP can be used as a promising protective agent against cytotoxic insults- or ROS-mediated TEC injury. Furthermore, our findings provide new insights into a therapeutic approach for the future application of FCP in the prevention and treatment of various types of oxidative- or cytotoxic stress-related cell injury in TECs as well as age-related or acute thymus involution.
Keyphrases
- signaling pathway
- reactive oxygen species
- pi k akt
- induced apoptosis
- cell death
- oxidative stress
- poor prognosis
- immune response
- cell cycle arrest
- epithelial mesenchymal transition
- dna damage
- liver failure
- single cell
- cell therapy
- amino acid
- bone marrow
- stress induced
- binding protein
- endoplasmic reticulum stress
- intensive care unit
- stem cells
- wound healing
- machine learning
- toll like receptor
- big data
- heat stress
- tissue engineering
- drug induced
- dendritic cells
- mesenchymal stem cells
- newly diagnosed
- electronic health record
- combination therapy
- current status
- inflammatory response
- long non coding rna