Developing a Multichannel Bioreactor with a Collagen Scaffold, ECM, and Cryoprecipitate to Significantly Produce Platelets from Umbilical Cord Blood Stem Cells

Mohamad Hosein Derakhty Gonbad, Ali Baradar Khoshfetrat, Ali Akbar Movassaghpour, Zohre Sanaat, Hojjatollah Nozad Charoudeh
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 Materials and Methods: In this study, the CD34 cells isolated from cord blood were differentiated into megakaryocytes. A 6-chamber bioreactor with a two-layer collagen scaffold, several ECM factors, and human cryoprecipitate were used to simulate the structure of the bone marrow. After the addition of megakaryocytes to the scaffold, PLTs were produced due to the flow pressure and the interaction between the scaffold structure and the ECM factors.
 Results: CD41 + cells were expanded 100 times as much as CD34 + cord blood stem cells. The mean PLT release from one megakaryocyte in the pure collagen scaffold was 17.42 PLTs. Once fibrin, fibronectin, hyaluronic acid, and cryoprecipitates were added to collagen, the mean PLT release was 21.4, 22.4, 23.9, and 27.37, respectively. With the simultaneous addition of three factors to collagen (CFFH) and then four factors (CFFHC), the number of PLTs reached 30.52 and then 34.
 Conclusion: Functional PLTs can be produced on a large scale with a multi-chamber bioreactor using a combination of ECM and cryoprecipitate with collagen scaffolding.","PeriodicalId":94048,"journal":{"name":"International journal of hematology-oncology and stem cell research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of hematology-oncology and stem cell research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/ijhoscr.v17i4.13916","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background: Platelets play a key role in the treatment of thrombocytopenia. Nowadays, platelets (PLTs) are only obtained through blood donation. However, due to the limitations in their preparation and storage, they are produced in laboratories, especially through bioreactors that convert megakaryocytes from stem cells into large-scale injectable PLTs. Materials and Methods: In this study, the CD34 cells isolated from cord blood were differentiated into megakaryocytes. A 6-chamber bioreactor with a two-layer collagen scaffold, several ECM factors, and human cryoprecipitate were used to simulate the structure of the bone marrow. After the addition of megakaryocytes to the scaffold, PLTs were produced due to the flow pressure and the interaction between the scaffold structure and the ECM factors. Results: CD41 + cells were expanded 100 times as much as CD34 + cord blood stem cells. The mean PLT release from one megakaryocyte in the pure collagen scaffold was 17.42 PLTs. Once fibrin, fibronectin, hyaluronic acid, and cryoprecipitates were added to collagen, the mean PLT release was 21.4, 22.4, 23.9, and 27.37, respectively. With the simultaneous addition of three factors to collagen (CFFH) and then four factors (CFFHC), the number of PLTs reached 30.52 and then 34. Conclusion: Functional PLTs can be produced on a large scale with a multi-chamber bioreactor using a combination of ECM and cryoprecipitate with collagen scaffolding.
利用胶原支架、ECM和低温沉淀构建多通道生物反应器,从脐带血干细胞中显著产生血小板
背景:血小板在治疗血小板减少症中起着关键作用。目前,血小板(PLTs)只能通过献血获得。然而,由于其制备和储存的局限性,它们是在实验室中生产的,特别是通过生物反应器将干细胞中的巨核细胞转化为大规模可注射的plt。材料与方法:从脐带血中分离CD34细胞,将其分化为巨核细胞。采用6室生物反应器,采用双层胶原支架、几种ECM因子和人低温沉淀模拟骨髓结构。巨核细胞加入支架后,由于流动压力和支架结构与ECM因子的相互作用,产生plt。 结果:CD41 +细胞扩增量是CD34 +脐带血干细胞的100倍。在纯胶原支架中,一个巨核细胞的平均PLT释放量为17.42个PLT。在胶原蛋白中加入纤维蛋白、纤维连接蛋白、透明质酸和低温沉淀物后,平均PLT释放量分别为21.4、22.4、23.9和27.37。同时加入三因子(CFFH)再加入四因子(CFFHC), PLTs的数量分别达到30.52个和34个。 结论:在多室生物反应器中,使用ECM和低温沉淀结合胶原支架,可以大规模生产功能性plt。
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