涉及新相互作用伙伴(RRAGC & PSMC2, CKAP4 & MANF, CTR9 & CNTNAP2)的造血活性调控

Pub Date : 2020-09-30 DOI:10.4236/cellbio.2020.93007
Swati Sharma, G. Gangenahalli, U. Singh
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引用次数: 0

摘要

造血干细胞(Hematopoietic stem cells, hsc)是由多种造血细胞因子和生长因子调控的组织特异性细胞,通过调节造血干细胞的功能活性影响早期祖细胞的存活、增殖和分化机制。在本研究中,三个新的基因对组合RRAGC & PSMC2;Ckap4 & manf;CTR9和CNTNAP2是新发现的。利用RT-PCR和sirna介导的基因敲低策略证实了这些新的基因组合,并在细胞因子组合(IL-3、FLT-3和SCF)存在下在K562人白血病细胞系中表达。这项研究表明基因对在不同的分子活动中发挥协同作用,如泛素化或蛋白酶体降解,钙动员,多巴胺信号传导。
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Regulation of Hematopoietic Activity Involving New Interacting Partners (RRAGC & PSMC2, CKAP4 & MANF and CTR9 & CNTNAP2)
Hematopoietic stem cells (HSCs) are tissue-specific cells giving rise to all mature blood cell types regulated by a diverse group of hematopoietic cytokines and growth factors that influences the survival & proliferation of early progenitors and differentiation mechanisms by modulating the functional activities of HSCs. In this study, the functional yet distinctive role of three novel combinations of gene pairs RRAGC & PSMC2; CKAP4 & MANF; and CTR9 & CNTNAP2 have been newly identified. These novel combinations of genes were confirmed and expressed in K562 human leukemic cell line in the presence of cytokine combination (IL-3, FLT-3 and SCF) using RT-PCR and siRNA-mediated gene knock down strategy. This study signifies the synergistic role of gene pairs in different molecular activities like ubiquitination or proteasomal degradation, calcium mobilization, dopamine signaling.
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