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首页> 外文期刊>Journal of Stem Cells and Regenerative Medicine >Defining Molecular Phenotypes of Mesenchymal and hematopoietic Stem Cells derived from Peripheral blood of Acute Lymphocytic Leukemia patients for regenerative stem cell therapy
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Defining Molecular Phenotypes of Mesenchymal and hematopoietic Stem Cells derived from Peripheral blood of Acute Lymphocytic Leukemia patients for regenerative stem cell therapy

机译:定义急性淋巴细胞白血病患者外周血来源的间充质和造血干细胞的分子表型,以进行再生干细胞治疗

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Acute Lymphocytic Leukemia (ALL) is a clonal myeloid disorder affecting all age groups, characterized by accumulation of immature blast cells in bone marrow and in peripheral blood. Autologous Bone Marrow Transplantation is a present treatment for cure of ALL patients, which is very expensive, invasive process and may have possibility of transplantation of malignant stem cells to patients. In the present study, we hypothesized to isolate large number of normal Mesenchymal & Hematopoietic stem cells from peripheral blood of ALL patients, which will be further characterized for their normal phenotypes by using specific molecular stem cell markers. This is the first study, which defines the existing phenotypes of isolated MSCs and HSCs from peripheral blood of ALL patients. We have established three cell lines in which two were Mesenchymal stem cells designated as MSCALL and MSCnsALL and one was suspension cell line designated as HSCALL. The HSCALL cell line was developed from the lymphocyte like cells secreted by MSCALL cells. Our study also showed that MSCALL from peripheral blood of ALL patient secreted hematopoietic stem cells in vitro culture. We have characterized all three-cell lines by 14 specific stem cell molecular markers. It was found that both MSC cell lines expressed CD105, CD13, and CD73 with mixed expression of CD34 and CD45 at early passage whereas, HSCALL cell line expressed prominent feature of hematopoietic stem cells such as CD34 and CD45 with mild expression of CD105 and CD13. All three-cell lines expressed LIF, OCT4, NANOG, SOX2, IL6, and DAPK. These cells mildly expressed COX2 and did not express BCR-ABL. Overall it was shown that isolated MSCs and HSCs can be use as a model system to study the mechanism of leukemia at stem cell level and their use in stem cell regeneration therapy for Acute Lymphocytic Leukemia.
机译:急性淋巴细胞白血病(ALL)是一种影响所有年龄段的克隆性骨髓疾病,其特征是未成熟的胚细胞在骨髓和外周血中积累。自体骨髓移植是目前用于治疗所有患者的治疗方法,这是非常昂贵的侵入性过程,并且可能具有将恶性干细胞移植至患者的可能性。在本研究中,我们假设从ALL患者的外周血中分离出大量正常的间充质和造血干细胞,将通过使用特定的分子干细胞标记物进一步表征其正常表型。这是第一项研究,该研究定义了ALL患者外周血中分离的MSC和HSC的现有表型。我们已经建立了三种细胞系,其中两种是间充质干细胞,分别命名为MSCALL和MSCnsALL,一种是悬浮细胞系,命名为HSCALL。 HSCALL细胞系由MSCALL细胞分泌的淋巴细胞样细胞发育而来。我们的研究还表明,ALL患者外周血中的MSCALL在体外培养中分泌了造血干细胞。我们已经通过14种特定的干细胞分子标记物对所有三细胞系进行了表征。已经发现,两种MSC细胞系在早期传代时均表达CD105,CD13和CD73,并具有CD34和CD45的混合表达,而HSCALL细胞系表达造血干细胞如CD34和CD45的显着特征,并具有CD105和CD13的轻度表达。所有三细胞系均表达LIF,OCT4,NANOG,SOX2,IL6和DAPK。这些细胞轻度表达COX2,不表达BCR-ABL。总的来说,已表明分离的MSC和HSC可以用作模型系统来研究干细胞水平上的白血病机制及其在急性淋巴细胞白血病干细胞再生治疗中的用途。

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