Mesenchymal Stem Cell Exosomes Derived from Feline Adipose Tissue Enhance the Effects of Anti-Inflammation Compared to Fibroblasts-Derived Exosomes.
Soo-Eun SungMin-Soo SeoKyung-Ku KangJoo-Hee ChoiSijoon LeeMinkyoung SungKilsoo KimGun Woo LeeJu-Hyeon LimSeung Yun YangSang-Gu YimSeul-Ki KimSangbum ParkYoung-Sam KwonSungho YunPublished in: Veterinary sciences (2021)
Adipose tissue-derived mesenchymal stem cells (AD-MSCs) release extracellular vesicles such as exosomes, apoptotic bodies, and microparticles. In particular, exosomes are formed inside cells via multivesicular bodies (MVBs), thus their protein, DNA, and RNA content are similar to those of the parent cells. Exosome research is rapidly expanding, with an increase in the number of related publications observed in recent years; therefore, the function and application of MSC-derived exosomes could emerge as cell-free therapeutics. Exosomes have been isolated from feline AD-MSCs and feline fibroblast cell culture media using ultracentrifugation. Feline exosomes have been characterized by FACS, nanoparticle tracking analysis, and transmission electron microscopy imaging. Moreover, cytokine levels were detected by sandwich enzyme-linked immunosorbent assay in exosomes and LPS-induced THP-1 macrophages. The size of the isolated exosomes was that of a typical exosome, i.e., approximately 150 nm, and they expressed tetraspanins CD9 and CD81. The anti-inflammatory factor IL-10 was increased in feline AD-MSC-derived exosomes. However, pro-inflammatory factors such as IL-1β, IL-8, IL-2, RANTES, and IFN-gamma were significantly decreased in feline AD-MSC-derived exosomes. This was the first demonstration that feline AD-MSC-derived exosomes enhance the inflammatory suppressive effects and have potential for the treatment of immune diseases or as an inflammation-inhibition therapy.
Keyphrases
- mesenchymal stem cells
- stem cells
- umbilical cord
- adipose tissue
- cell free
- bone marrow
- lps induced
- oxidative stress
- induced apoptosis
- type diabetes
- anti inflammatory
- cell death
- immune response
- cell therapy
- metabolic syndrome
- high resolution
- photodynamic therapy
- signaling pathway
- dendritic cells
- cell proliferation
- extracellular matrix
- binding protein
- amino acid