RETRACTED: Bone marrow mesenchymal stem cells combined with Atractylodes macrocephala polysaccharide attenuate ulcerative colitis (Retracted Article)
被引:8
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作者:
Zheng, Zhijuan
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Shandong Univ Tradit Chinese Med, Expt Ctr, Key Lab Tradit Chinese Med Class Theory, Shandong Prov Key Lab Tradit Chinese Med Basic Re, Jinan, Peoples R ChinaShandong Univ Tradit Chinese Med, Expt Ctr, Key Lab Tradit Chinese Med Class Theory, Shandong Prov Key Lab Tradit Chinese Med Basic Re, Jinan, Peoples R China
Zheng, Zhijuan
[1
]
Wang, Junqing
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Shandong Univ Tradit Chinese Med, Coll Hlth Sci, Jinan, Peoples R ChinaShandong Univ Tradit Chinese Med, Expt Ctr, Key Lab Tradit Chinese Med Class Theory, Shandong Prov Key Lab Tradit Chinese Med Basic Re, Jinan, Peoples R China
Wang, Junqing
[2
]
机构:
[1] Shandong Univ Tradit Chinese Med, Expt Ctr, Key Lab Tradit Chinese Med Class Theory, Shandong Prov Key Lab Tradit Chinese Med Basic Re, Jinan, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Coll Hlth Sci, Jinan, Peoples R China
The aim of the present study was to explore the effects of bone marrow mesenchymal stem cells (BMSCs), combined with Atractylodes macrocephala polysaccharide (AMP), in an experimental model of ulcerative colitis. BMSCs were first isolated, cultured, and identified by flow cytometry. A rat model of colitis was established by trinitrobenzene sulfonic acid (TNBS) injection. Rats were treated with BMSCs with or without AMP for 1 or 2 weeks. H&E staining was performed to assess the extent of histological injury. IEC-6 and BMSCs were co-cultured and treated with AMP. Cell migration was measured using the Transwell assay, whilst the levels of cytokines in the rat blood samples were detected using ELISA. In addition, cytokine levels in the cell supernatant were measured by microarray. The results showed that BMSCs were successfully isolated. BMSCs treatment could markedly alleviate injury according to histological analysis and regulate inflammatory cytokine production in this rat model of TNBS-induced colitis, where a higher number of BMSCs was found in the intestinal tract, compared to the model. AMP not only potentiated the effects of BMSCs on preventing TNBS-induced colitis but also promoted BMSC homing to the injured tissue and regulated cytokines. Furthermore, BMSCs and AMP promoted the migration of IEC in vitro and influenced multiple genes. In conclusion, AMP treatment improved the therapeutic effects of BMSCs on ulcerative colitis, potentially providing a novel clinical treatment strategy for colitis.
机构:
Natl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, IranNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Razeghian, Ehsan
Margiana, Ria
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Univ Indonesia, Fac Med, Dept Anat, Jakarta, Indonesia
Natl Referral Hosp, Cipto Mangunkusumo Hosp, Cent Jakarta, Indonesia
Univ Indonesia, Fac Med, Masters Programme Biomed Sci, Jakarta, IndonesiaNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Margiana, Ria
Chupradit, Supat
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Chiang Mai Univ, Fac Associated Med Sci, Dept Occupat Therapy, Chiang Mai, ThailandNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Chupradit, Supat
Bokov, Dmitry O.
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Sechenov First Moscow State Med Univ, Inst Pharm, Moscow, Russia
Fed Res Ctr Nutr Biotechnol & Food Safety, Lab Food Chem, Moscow, RussiaNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Bokov, Dmitry O.
Abdelbasset, Walid Kamal
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Prince Sattam Bin Abdulaziz Univ, Coll Appl Med Sci, Dept Hlth & Rehabil Sci, Al Kharj, Saudi Arabia
Cairo Univ, Kasr Al Aini Hosp, Dept Phys Therapy, Giza, EgyptNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Abdelbasset, Walid Kamal
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Marofi, Faroogh
Shariatzadeh, Siavash
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Shahid Beheshti Univ Med Sci, Sch Med, Dept Pharmacol, Tehran, IranNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
Shariatzadeh, Siavash
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Tosan, Foad
Jarahian, Mostafa
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German Canc Res Ctr, Toxicol & Chemotherapy Unit G401, Heidelberg, GermanyNatl Inst Genet Engn & Biotechnol NIGEB, Med Biotechnol Dept, Human Genet Div, Tehran, Iran
机构:
Shanghai Punan Hosp Pudong New Dist, Orthopaed, Shanghai 200125, Peoples R ChinaShanghai Punan Hosp Pudong New Dist, Orthopaed, Shanghai 200125, Peoples R China
机构:
Zhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Ling, Shiyong
Luo, Xi
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机构:
Second Mil Med Univ, Changzheng Hosp, Spine Ctr, Dept Orthoped Surg, Shanghai 200003, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Luo, Xi
Lv, Bo
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Zhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Lv, Bo
Wang, Hua
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Zhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Wang, Hua
Xie, Mengzhi
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Zhabei Cent Hosp, Dept Radiol, Shanghai 200070, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Xie, Mengzhi
Huang, Kai
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Zhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
Huang, Kai
Sun, Jingchuan
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Second Mil Med Univ, Changzheng Hosp, Spine Ctr, Dept Orthoped Surg, Shanghai 200003, Peoples R ChinaZhabei Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China