Bhattacharjee Jashdeep, Das Barun, Mishra Alaknanda, Sahay Preeti, Upadhyay Pramod
Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital Los Angeles, Los Angeles, CA, USA.
National Institute of Immunology, New Delhi , India.
F1000Res. 2017 Nov 23;6:2045. doi: 10.12688/f1000research.12802.3. eCollection 2017.
: Magnetic sorting of cells, based on microbead conjugated antibodies (Abs), employs positive as well as negative immunomagnetic separation methods, for isolation of a specific cell population. These microbeads are suggested to be nontoxic, biodegradable carriers conjugated to various antibodies. Isolation of cells through positive selection involves the attachment of antibody conjugated microbeads to the cells of interest, followed by their isolation in the presence of a strong magnetic field to obtain higher purity. Negative selection involves attachment of microbead conjugated antibodies to all other cell populations except the cells of interest, which remain untagged. In the present study, we compared the two methods for their effect on functional and immunophenotypic behavior of isolated CD14+ monocytes. : Peripheral blood mononuclear cells (PBMCs) were isolated from blood collected from healthy volunteers by density gradient centrifugation. Human blood derived monocytes were isolated through positive selection and negative selection, making use of the appropriate monocyte isolation kit. Monocytes were then stimulated with lipopolysaccharide (LPS) and their activation and proliferation capacity were examined. The degradation or dissociation of cell-bound microbeads was also investigated. : We observed an impaired LPS sensitivity as well as poor activation and proliferation capacity upon stimulation by LPS in positively sorted CD14+ monocytes as compared to negatively sorted CD14+ monocytes. The attached microbeads did not degrade and remained attached to the cells even after 6 days of culture. : Our results suggest that positively sorted CD14+ cells exhibit hampered functionality and may result in inaccurate analysis and observations in downstream applications. However, these cells can be used for immediate analytical procedures.
基于与抗体(Abs)偶联的微珠对细胞进行磁性分选,采用阳性和阴性免疫磁珠分离方法来分离特定的细胞群体。这些微珠被认为是与各种抗体偶联的无毒、可生物降解的载体。通过阳性选择分离细胞涉及将与抗体偶联的微珠附着到感兴趣的细胞上,然后在强磁场存在下进行分离以获得更高的纯度。阴性选择涉及将与微珠偶联的抗体附着到除感兴趣的细胞之外的所有其他细胞群体上,而感兴趣的细胞保持未标记状态。在本研究中,我们比较了这两种方法对分离的CD14 +单核细胞的功能和免疫表型行为的影响。:通过密度梯度离心从健康志愿者采集的血液中分离外周血单核细胞(PBMC)。利用适当的单核细胞分离试剂盒,通过阳性选择和阴性选择分离人血来源的单核细胞。然后用脂多糖(LPS)刺激单核细胞,并检测其活化和增殖能力。还研究了细胞结合的微珠的降解或解离情况。:我们观察到,与阴性分选的CD14 +单核细胞相比,阳性分选的CD14 +单核细胞对LPS刺激的敏感性受损,活化和增殖能力也较差。即使在培养6天后,附着的微珠也没有降解,仍然附着在细胞上。:我们的结果表明,阳性分选的CD14 +细胞表现出功能障碍,可能会导致下游应用中的分析和观察不准确。然而,这些细胞可用于即时分析程序。