Exosomes Derived from Human Umbilical Cord Mesenchymal Stem Cells Alleviate Psoriasis-like Skin Inflammation.
Yuli ZhangJianjun YanZhengjun LiJuan ZhengQing SunPublished in: Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research (2022)
Immunomodulatory effects of mesenchymal stem cells (MSCs) in inflammatory diseases, including psoriasis, are well documented. However, the role of MSC-derived exosomes (MSCs-Exo) in psoriasis-like skin inflammation remains largely unknown. This study aimed to investigate whether MSCs-Exo play a regulatory role in psoriasis-like skin inflammation. We found that subcutaneous injection of human umbilical cord MSCs-Exo (hucMSCs-Exo) significantly suppressed the proliferation of epidermis and reduced Psoriasis Area and Severity Index (PASI) scores in imiquimod (IMQ)-induced mice. hucMSCs-Exo also reduced the expression of interleukin (IL)-17, IL-23, and chemokine C-C-motif ligand 20 (CCL20) and inhibited phosphorylation of signal transducer and activator of transcription 3 (STAT3) in the skin of IMQ-induced mice and in human keratinocyte (HaCaT) cells. In addition, co-cultured with hucMSCs-Exo in vitro , the maturation and activation of dendritic cells (DCs) were suppressed, and the expression level of IL-23 was decreased. These results indicate that hucMSCs-Exo can effectively ameliorate psoriasis-like skin inflammation in mice by regulating the expression of IL-23 and IL-17, and inhibiting the maturation and activation of DCs. Our data offer a promising therapeutic approach for psoriasis by leveraging the immunomodulatory effects of hucMSCs-Exo.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- endothelial cells
- oxidative stress
- poor prognosis
- bone marrow
- high glucose
- soft tissue
- dendritic cells
- cell therapy
- atopic dermatitis
- diabetic rats
- wound healing
- induced pluripotent stem cells
- pluripotent stem cells
- immune response
- transcription factor
- high fat diet induced
- stem cells
- signaling pathway
- cell proliferation
- metabolic syndrome
- binding protein
- inflammatory response
- insulin resistance
- toll like receptor
- regulatory t cells
- adipose tissue
- cell cycle arrest
- long non coding rna
- big data
- drug induced
- liver fibrosis
- wild type
- artificial intelligence
- nuclear factor
- pi k akt