The secretome of periodontal ligament stem cells from MS patients protects against EAE

被引:103
作者
Rajan, Thangavelu Soundara [1 ]
Giacoppo, Sabrina [1 ]
Diomede, Francesca [2 ]
Ballerini, Patrizia [3 ]
Paolantonio, Michele [2 ]
Marchisio, Marco [4 ]
Piattelli, Adriano [2 ]
Bramanti, Placido [1 ]
Mazzon, Emanuela [1 ]
Trubiani, Oriana [2 ]
机构
[1] IRCCS Ctr Neurolesi Bonino Pulejo, Via Provinciale Palermo, I-98124 Messina, Italy
[2] Univ G DAnnunzio, Stem Cells & Regenerat Med Lab, Dept Med Oral & Biotechnol Sci, Via Vestini 31, I-66100 Chieti, Italy
[3] Univ G DAnnunzio, Dept Psychol Hlth & Terr Sci, Via Vestini 31, I-66100 Chieti, Italy
[4] Univ G DAnnunzio, Dept Med & Aging Sci, Via Vestini 31, I-66100 Chieti, Italy
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; HUMAN BONE-MARROW; EXTRACELLULAR VESICLES; IN-VITRO; CONDITIONED MEDIUM; EXOSOMES; MECHANISMS; MICE; VIVO; MODULATION;
D O I
10.1038/srep38743
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Manipulation of stem cells or stem cells-derived secretome has emerged as a novel alternative therapeutic option for multiple sclerosis (MS). Here we show that human periodontal ligament stem cells (hPDLSCs)-derived conditioned medium (hPDLSCs-CM) and purified exosomes/microvesicles (hPDLSCs-EMVs) obtained from Relapsing Remitting (RR)-MS patients and healthy donors block experimental autoimmune encephalomyelitis (EAE), a mouse model of MS, by inducing anti-inflammatory and immunosuppressive effects in spinal cord and spleen, and reverse disease progression by restoring tissue integrity via remyelination in the spinal cord. We show that hPDLSCs-CM and hPDLSCs-EMVs reduce pro-inflammatory cytokines IL-17, IFN-gamma, IL-1 beta, IL-6, TNF-alpha, and induce anti-inflammatory IL-10. In addition, apoptosis related STAT1, p53, Caspase 3, and Bax expressions were attenuated. Our findings unravel the immunosuppressive effects of hPDLSCs-CM and hPDLSCs-EMVs in EAE mice, and suggest simple alternative autologous source for patient-customized cell-free targeting treatment in MS patients.
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页数:16
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