首页> 外国专利> REPROGRAMMING HUMAN ENDOTHELIUM IN HEMATOPOIETIC PRECURSORS OF MULTIPLE LINES OF DIFFERENTIATION USING CERTAIN FACTORS

REPROGRAMMING HUMAN ENDOTHELIUM IN HEMATOPOIETIC PRECURSORS OF MULTIPLE LINES OF DIFFERENTIATION USING CERTAIN FACTORS

机译:使用某些因素在多系分化造血前体中重编程人内皮

摘要

FIELD: pharmaceuticals.;SUBSTANCE: invention refers to pharmaceutical industry, namely to a method for producing hematopoietic precursors of differentiation lines (HMLP) from endothelial cells (EC). A method for producing human HMLP from human EC, involving culturing EC, transduced by one or more vectors triggering the expression of each of the transcription factors: homologue B of osteosarcoma virus oncogene of mouse Finkel-Biskis-Jinkins (FOSB) or functional derivative thereof, having at least 90 % amino acid sequence FOSB identity, growth factor-independent transcriptional repressor 1 (GFI1) or functional derivative thereof, having at least 90 % amino acid sequence identity of GFI1, Runt-related transcription factor 1 (RUNX1) or its functional derivative, having at least 90 % amino acid sequence identity RUNX1, provisional oncogene of integrating a virus forming foci in spleen, (SPI1) or its functional derivative, having at least 90 % amino acid sequence identity SPI1, in a serum-free haemopoietic medium with endothelial feeder cells transformed for expression of either the open reading frame 1 E4 adenovirus (E4ORF1) gene or the Akt gene. A HMLP population for intravenous infusion to a patient with hematopoietic disorder. A composition for intravenous infusion to a patient with hematopoietic disorder. A method of treating hematopoietic disorder.;EFFECT: disclosed method enables to obtain HMLP with a mixture of cell types, wherein each cell type has separate cell markers and / or a separate level of differentiation.;23 cl, 28 dwg, 1 tbl
机译:技术领域本发明涉及制药工业,即从内皮细胞(EC)生产分化系(HMLP)的造血前体的方法。一种由人EC产生人HMLP的方法,包括培养由一种或多种触发每个转录因子表达的载体转导的EC:小鼠Finkel-Biskis-Jinkins(FOSB)的骨肉瘤病毒癌基因同源物B或其功能衍生物,具有至少90%的氨基酸序列FOSB同一性,不依赖生长因子的转录阻遏物1(GFI1)或其功能衍生物,具有至少90%的氨基酸的GFI1,Runt相关转录因子1(RUNX1)或其同源性具有至少90%氨基酸序列同一性RUNX1的功能性衍生物,在无血清造血细胞中整合病毒在脾脏中形成病灶的临时致癌基因(SPI1)或其功能衍生物,具有至少90%氨基酸序列同一性SPI1含有内皮饲养细胞的培养基,用于表达开放阅读框1 E4腺病毒(E4ORF1)基因或Akt基因。用于向造血系统疾病患者静脉输液的HMLP人群。用于向造血系统疾病患者静脉内输注的组合物。一种治疗造血疾病的方法;效果:所公开的方法能够获得具有多种细胞类型混合物的HMLP,其中每种细胞类型具有单独的细胞标志物和/或单独的分化水平。23cl,28 dwg,1 tbl

著录项

  • 公开/公告号RU2691062C2

    专利类型

  • 公开/公告日2019-06-10

    原文格式PDF

  • 申请/专利权人 KORNELL YUNIVERSITI;

    申请/专利号RU20150134394

  • 申请日2014-01-15

  • 分类号A61K35/44;A61P7/02;A61P35/02;C12N5/073;

  • 国家 RU

  • 入库时间 2022-08-21 11:46:11

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