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用于转化外周血单个核细胞和提取 DNA 的全血采集和处理:1 型糖尿病遗传学联合会。

Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium.

机构信息

Division of Endocrinology and Diabetes, Department of Internal Medicine, Ulm University, Ulm, Germany.

出版信息

Clin Trials. 2010;7(1 Suppl):S65-74. doi: 10.1177/1740774510373493. Epub 2010 Jul 1.

Abstract

BACKGROUND

and

PURPOSE

To yield large amounts of DNA for many genotype analyses and to provide a renewable source of DNA, the Type 1 Diabetes Genetics Consortium (T1DGC) harvested DNA and peripheral blood mononuclear cells (PBMCs) from individuals with type 1 diabetes and their family members in several regions of the world.

METHODS

DNA repositories were established in Asia-Pacific, Europe, North America, and the United Kingdom. To address region-specific needs, different methods and sample processing techniques were used among the laboratories to extract and to quantify DNA and to establish Epstein-Barr virus transformed cell lines.

RESULTS

More than 98% of the samples of PBMCs were successfully transformed. Approximately 20-25 microg of DNA were extracted per mL of whole blood. Extraction of DNA from the cell pack ranged from 92 to 165 microg per cell pack. In addition, the extracted DNA from whole blood or transformed cells was successfully utilized in each regional human leukocyte antigen genotyping laboratory and by several additional laboratories performing consortium-wide genotyping projects.

LIMITATIONS

Although the isolation of PBMCs was consistent among sites, the measurement of DNA was difficult to harmonize.

CONCLUSIONS

DNA repositories can be established in different regions of the world and produce similar amounts of high-quality DNA for a variety of high-throughput genotyping techniques. Furthermore, even with the distances and time necessary for transportation, highly efficient transformation of PBMCs is possible. For future studies/trials involving several laboratories in different locations, the T1DGC experience includes examples of protocols that may be applicable. In summary, T1DGC has developed protocols that would be of interest to any scientific organization attempting to overcome the logistical problems associated with studies/trials spanning multiple research facilities, located in different regions of the world.

摘要

背景

目的

为了进行大量的基因型分析并提供可再生的 DNA 来源,1 型糖尿病遗传学联合会(T1DGC)从世界各地的 1 型糖尿病患者及其家庭成员中采集了 DNA 和外周血单核细胞(PBMC)。

方法

在亚太地区、欧洲、北美和英国建立了 DNA 库。为了满足区域特定需求,实验室之间使用了不同的方法和样本处理技术来提取和定量 DNA,并建立了 Epstein-Barr 病毒转化的细胞系。

结果

超过 98%的 PBMC 样本成功转化。每毫升全血可提取约 20-25 微克的 DNA。从细胞包中提取的 DNA 每个细胞包的范围为 92 至 165 微克。此外,从全血或转化细胞中提取的 DNA 成功地用于每个区域的人类白细胞抗原基因分型实验室以及几个执行联盟范围基因分型项目的额外实验室。

局限性

尽管 PBMC 的分离在各个站点之间是一致的,但 DNA 的测量难以协调。

结论

可以在世界不同地区建立 DNA 库,并为各种高通量基因分型技术生产类似数量的高质量 DNA。此外,即使需要运输的距离和时间,PBMC 的高效转化也是可行的。对于涉及不同地点的多个实验室的未来研究/试验,T1DGC 的经验包括可能适用的协议示例。总之,T1DGC 制定的协议对于任何试图克服跨越多个研究设施、位于世界不同地区的研究/试验相关的后勤问题的科学组织都将具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c260/2917848/cb10c9c7de4e/10.1177_1740774510373493-fig1.jpg

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