2020
DOI: 10.3390/biomedicines8100439
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Anti-Inflammatory Effects of M-MSCs in DNCB-Induced Atopic Dermatitis Mice

Abstract: Atopic dermatitis (AD) is an inflammatory skin disease caused by an imbalance between Th1 and Th2 cells. AD patients suffer from pruritus, excessive dryness, red or inflamed skin, and complications such as sleep disturbances and depression. Although there are currently many AD treatments available there are insufficient data on their long-term stability and comparative effects. Moreover, they have limitations due to various side effects. Multipotent mesenchymal stem cells (M-MSCs) might have potential for next… Show more

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Cited by 11 publications
(16 citation statements)
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“…MSC-derived exosomes have the potential for therapeutic application in wound healing via tissue regeneration and regulation of immune response and inflammation [ 42 ]. It has been reported that secretion of MSCs with anti-inflammatory properties has beneficial effects on atopic dermatitis-related inflammatory lesions, such as pruritus [ 43 ], but the effects of exosomes on itching have not been studied. Previous studies have demonstrated that exosomes derived from MSCs could accelerate normal and diabetic wound healing [ 2 , 44 , 45 ].…”
Section: Discussionmentioning
confidence: 99%
“…MSC-derived exosomes have the potential for therapeutic application in wound healing via tissue regeneration and regulation of immune response and inflammation [ 42 ]. It has been reported that secretion of MSCs with anti-inflammatory properties has beneficial effects on atopic dermatitis-related inflammatory lesions, such as pruritus [ 43 ], but the effects of exosomes on itching have not been studied. Previous studies have demonstrated that exosomes derived from MSCs could accelerate normal and diabetic wound healing [ 2 , 44 , 45 ].…”
Section: Discussionmentioning
confidence: 99%
“…Secretion was confirmed. [ 13 ] Based on these results, it was expected that M-MSCs would have the ability to control inflammation through the paracrine effect, so cells were injected into the muscle instead of the completely amputated tendon. To demonstrate these characteristics of the M-MSCs in transcriptomic level, the cells were compared with BM-MSCs and hDFs.…”
Section: Discussionmentioning
confidence: 99%
“…The M-MSCs were obtained from embryoid bodies (EBs) of hPSCs as previously described [ 12 , 13 ]. Briefly, SNUhES cells between passage 40–60 were cultured in DMEM/F-12 Medium supplemented with 20% knockout serum replacement, 1 mM glutamine, 0.1 mM β-mercaptoethanol, 0.1 mM nonessential amino acids, and 4 ng/mL human recombinant bFGF, all of which were purchased from Invitrogen Corporation (Carlsbad, CA, USA) (hPSC culture media).…”
Section: Methodsmentioning
confidence: 99%
“…In addition to GVHD, an increasing number of studies and approximately a thousand MSC clinical trials ramify to most medical specialties, especially cardiovascular medicine, neurology, autoimmune diseases, and musculoskeletal diseases, highlighting that the application potential of MSCs is far from being exhausted [ 6 ]. Therefore, a review covering MSC therapy for nonischemic dilated cardiomyopathy (NIDCM) [ 7 ] and a research article developing MSCs as the next-generation cell-based therapeutics for atopic dermatitis (AD) [ 8 ] are included in this Special Issue.…”
mentioning
confidence: 99%
“…Secretions of hESC-derived multipotent MSCs were used to treat a mouse model of AD, showing the utility of hESC-derived multipotent MSCs as an immunoregulator having a significant relief effect in acute AD confirmed by protein expression and histological analyses. Being natural humoral immune regulators, MSC-based therapeutics may stand superior to conventional therapeutics, such as corticosteroids and antihistamines that are subject to various side effects [ 8 ].…”
mentioning
confidence: 99%