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生长抑素对人脐血CD34+细胞增殖能力的影响 被引量:3

Effects of somatostatin on proliferation ability of human CD34+ cells derived from umbilical cord blood*
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摘要 目的探索生长抑素(SST)对造血干/祖细胞增殖能力的影响以及可能机制。方法采用免疫磁殊分选技术纯化人脐血CD34^+细胞;SST孵育人CD34^+细胞后,体外集落形成、扩增培养了解细胞增殖;ELISA测定细胞内外TNF-α、TGF-β水平;RT—PCR分析其受体亚型。结果在1×10^-6~1×10^-10mol/L浓度范围内,SST抑制人CD34^+细胞集落形成及扩增倍数,其细胞集落形成抑制与SST浓度呈正相关(r=0.903,P〈0.01)。SST使CD34^+细胞内、外TNF-α及TGF-β1浓度显著增加(P〈0.05);人脐血CD34^+细胞表达SST-3型受体。结论SST通过人脐血CD34^+细胞上SST-3型受体介导,提高造血抑制因子TNF-α、TGF-β水平,抑制人CD34^+细胞的增殖、维持其干细胞特性。 Objective To investigate the effects and mechanisms of somatostatin (SST) on proliferation ability of hematopoietie/ progenitor stem ceils (HSC). Methods Mononuclear cell (MNC) derived from human cord blood was isolated by Ficoll, then MACS assay was used to purify human CD34^+ cells from MNC; After treated with SST, colony forming unit (CFU) enumeration and amplification were clone to assess the effects on proliferation of human CD34^+ cells;TNF-α and TGF-β in human CD34^+ cells or its supernatant were measured with ELISA;reverse transcriptation polymerase chain reaction was used to quantify receptor for SST (SSTR) and detected its subtype. Results SST in concentration of1×10^-6~1×10^-10mol/L inhibite proliferation of human CD34^+ cells. The inhibition of CFU forming bore a positive relation with the concentration of SST(r=0. 903,P〈0.01). The concentrations of TNF-α or TGF-β1 in human CD34^+ cells treated with SST were increased when compared to control group(P〈 0.05). Human CD34^+ cells expressed receptor for SST-3. Conclusion Mediated by SSTR-3 in Human CD34^+ cells,SST inhibite proliferation of Human CD34^+ cells due to increasing the intra cell concentrations of TNF-α and TGF-β, the inhibitive cytokines for hematopoiesis. SST tends to keep characteristics of Human CD34^+ cells and inhibit the differentiation of Human CD34^+ cells to granuloeyte-monocytes.
出处 《重庆医学》 CAS CSCD 北大核心 2009年第14期1728-1729,1731,共3页 Chongqing medicine
基金 国家杰出青年基金资助项目(39725012)。
关键词 造血干细胞 生长抑素 造血抑制 hematopoietic stem cells somatostatin inhibitive cytokines for hematopoiesis
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