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从肿瘤组织和外周血中分离人髓样树突状细胞。

Isolation of human myeloid dendritic cells from tumor tissue and peripheral blood.

作者信息

Brocks Carsten, Graefe Hendrik, Frenzel Henning, Pries Ralph, Wollenberg Barbara

机构信息

Department of Otorhinolaryngology, University of Schleswig-Holstein Campus Lübeck, 23538 Lübeck, Germany.

出版信息

In Vivo. 2006 Mar-Apr;20(2):239-42.

Abstract

BACKGROUND

Human myeloid dendritic cells (MDC) have been identified in human solid tumor tissue of head and neck squamous cell carcinoma (HNSCC), their cellular functions being strongly affected in this environment. The characterization of MDC differentiation and functions requires the establishment of highly efficient isolation procedures.

MATERIALS AND METHODS

Human MDC were isolated from peripheral blood and solid HNSCC using density gradient centrifugation or preparation of single cell suspensions, respectively. The cells were isolated by "magnetic bead separation" using magnetically-labelled antibodies and were analyzed by flow cytometry.

RESULTS

The isolation of human MDC from peripheral blood or solid HNSCC tissue resulted in highly enriched cell populations and revealed cell purities of about 90%.

CONCLUSION

The scale of molecular investigations on human myeloid dendritic cells is restricted by the limited proportion of this cell type. Thus, highly efficient and gentle MDC isolation procedures are essential to characterize in vivo matured MDC.

摘要

背景

在头颈部鳞状细胞癌(HNSCC)的实体瘤组织中已鉴定出人类髓样树突状细胞(MDC),其细胞功能在此环境中受到强烈影响。MDC分化和功能的表征需要建立高效的分离程序。

材料与方法

分别使用密度梯度离心法或制备单细胞悬液,从外周血和实体HNSCC中分离人类MDC。使用磁标记抗体通过“磁珠分离”法分离细胞,并通过流式细胞术进行分析。

结果

从外周血或实体HNSCC组织中分离人类MDC可得到高度富集的细胞群体,细胞纯度约为90%。

结论

对人类髓样树突状细胞的分子研究规模受到该细胞类型有限比例的限制。因此,高效且温和的MDC分离程序对于表征体内成熟的MDC至关重要。

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