The Therapeutic Efficacy of Adipose Tissue-Derived Mesenchymal Stem Cell Conditioned Medium on Experimental Colitis Was Improved by the Serum From Colitis Rats

被引:12
作者
Qi, Li-li [1 ]
Fan, Zhe-yu [1 ]
Mao, Hai-guang [1 ]
Wang, Jin-bo [1 ]
机构
[1] NingboTech Univ, Sch Biol & Chem Engn, Ningbo, Peoples R China
基金
中国国家自然科学基金;
关键词
adipose tissue-derived mesenchymal stem cell; serum from colitis model rat; conditioned medium; inflammatory bowel disease; therapeutic efficacy; ULCERATIVE-COLITIS; STROMAL CELLS; BONE-MARROW; MICROBIOTA; LUNG;
D O I
10.3389/fbioe.2021.694908
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Adipose derived mesenchymal stem cells (AD-MSCs) have shown therapeutic potential in treatments of inflammatory bowel disease (IBD). Due to the harsh host environment and poor survival of the cells, controversy concerning the homing, proliferation and differentiation of MSCs in lesion tissue still remains. It has been reported that conditioned media from MSCs could improve the colitis, whereas the therapeutic efficiency could be significantly elevated by the stimulation of pro-cytokines. In this study, we pre-treated the adipose derived MSCs with the serum from colitis rats and then the activated conditioned media (CM-AcMSC) were collected. To compare the therapeutic effects of CM-MSC and CM-AcMSC on IBD, we constructed dextran sodium sulphate (DSS)-induced colitis rat models. The colitis was induced in rats by administrating 5% DSS in drinking water for 10 days, and the disease symptoms were recorded daily. The colon histopathological changes were observed by different staining methods (H&E and PAS). The expression levels of MUC2 and tight junctions (TJs) were determined by RT-qPCR. The levels of inflammatory cytokines were analyzed by ELISA and western blot analysis. Our findings suggested that CM-AcMSC was more effective in ameliorating the clinical features and histological damage scores. Treatment with CM-AcMSC significantly increased the expression of MUC2 and TJs and suppressed the production of pro-inflammatory cytokines in colonic tissues of colitis rats. The inhibitory effects of CM-AcMSC on inflammatory responses of colitis rats were mediated by NF-kappa B signaling pathway. These results suggested that pre-activation of MSCs with serum from colitis rats could promote the production of paracrine factors and improve the therapeutic effects of conditioned medium on colitis rats.
引用
收藏
页数:12
相关论文
共 52 条
[1]   Mesenchymal stem cells: immune evasive, not immune privileged [J].
Ankrum, James A. ;
Ong, Joon Faii ;
Karp, Jeffrey M. .
NATURE BIOTECHNOLOGY, 2014, 32 (03) :252-260
[2]   The Severity of Dextran Sodium Sulfate-Induced Colitis Can Differ Between Dextran Sodium Sulfate Preparations of the Same Molecular Weight Range [J].
Bamba, Shigeki ;
Andoh, Akira ;
Ban, Hiromitsu ;
Imaeda, Hirotsugu ;
Aomatsu, Tomoki ;
Kobori, Ayako ;
Mochizuki, Yosuke ;
Shioya, Makoto ;
Nishimura, Takashi ;
Inatomi, Osamu ;
Sasaki, Masaya ;
Saitoh, Yasuharu ;
Tsujikawa, Tomoyuki ;
Araki, Yoshio ;
Fujiyama, Yoshihide .
DIGESTIVE DISEASES AND SCIENCES, 2012, 57 (02) :327-334
[3]   Endoscopic Administration of Mesenchymal Stromal Cells Reduces Inflammation in Experimental Colitis [J].
Barnhoorn, Marieke ;
de Jonge-Muller, Eveline ;
Molendijk, Ilse ;
van Gulijk, Mandy ;
Lebbink, Oscar ;
Janson, Stef ;
Schoonderwoerd, Mark ;
van der Helm, Danny ;
van der Meulen-de Jong, Andrea ;
Hawinkels, Lukas ;
Verspaget, Hein .
INFLAMMATORY BOWEL DISEASES, 2018, 24 (08) :1755-1767
[4]   The genetics and immunopathogenesis of inflammatory bowel disease [J].
Cho, Judy H. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (06) :458-466
[5]   Update on anti-tumor necrosis factor agents and other new drugs for inflammatory bowel disease [J].
Cohen, Benjamin L. ;
Sachar, David B. .
BMJ-BRITISH MEDICAL JOURNAL, 2017, 357
[6]   MicroRNA-193a-3p Reduces Intestinal Inflammation in Response to Microbiota via Down-regulation of Colonic PepT1 [J].
Dai, Xin ;
Chen, Xi ;
Chen, Qun ;
Shi, Lei ;
Liang, Hongwei ;
Zhou, Zhen ;
Liu, Qian ;
Pang, Wenjing ;
Hou, Dongxia ;
Wang, Cheng ;
Zen, Ke ;
Yuan, Yaozong ;
Zhang, Chen-Yu ;
Xia, Lu .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (26) :16099-16115
[7]   Autologous bone marrow-derived mesenchymal stromal cell treatment for refractory luminal Crohn's disease: results of a phase I study [J].
Duijvestein, Marjolijn ;
Vos, Anne Christine W. ;
Roelofs, Helene ;
Wildenberg, Manon E. ;
Wendrich, Barbara B. ;
Verspaget, Henricus W. ;
Kooy-Winkelaar, Engelina M. C. ;
Koning, Frits ;
Zwaginga, Jaap Jan ;
Fidder, Herma H. ;
Verhaar, Auke P. ;
Fibbe, Willem E. ;
van den Brink, Gijs R. ;
Hommes, Daniel W. .
GUT, 2010, 59 (12) :1662-1669
[8]   Insights into the Secretome of Mesenchymal Stem Cells and Its Potential Applications [J].
Eleuteri, Sharon ;
Fierabracci, Alessandra .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (18)
[9]   A Phase 2 Study of Allogeneic Mesenchymal Stromal Cells for Luminal Crohn's Disease Refractory to Biologic Therapy [J].
Forbes, Geoffrey M. ;
Sturm, Marian J. ;
Leong, Rupert W. ;
Sparrow, Miles P. ;
Segarajasingam, Dev ;
Cummins, Adrian G. ;
Phillips, Michael ;
Herrmann, Richard P. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2014, 12 (01) :64-71
[10]   Toll-like receptor 3 pre-conditioning increases the therapeutic efficacy of umbilical cord mesenchymal stromal cells in a dextran sulfate sodium-induced colitis model [J].
Fuenzalida, Patricia ;
Kurte, Monica ;
Fernandez-O'Ryan, Catalina ;
Ibanez, Cristina ;
Gauthier-Abeliuk, Melanie ;
Maria Vega-Letter, Ana ;
Gonzalez, Paz ;
Irarrazabal, Carlos ;
Quezada, Nataly ;
Figueroa, Fernando ;
Carrion, Flavio .
CYTOTHERAPY, 2016, 18 (05) :630-641