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冷冻保存的人单核细胞的抗体依赖性细胞介导的细胞毒性

Antibody-dependent cell-mediated cytotoxicity of cryopreserved human monocytes.

作者信息

Shah V O, McCarley D L, Weiner R S

出版信息

Cryobiology. 1984 Oct;21(5):475-9. doi: 10.1016/0011-2240(84)90044-0.

Abstract

Human peripheral blood monocytes (PBM) modulate and participate in a variety of host defences. Cryopreservation of PBM has facilitated studies of their function. Peripheral blood samples cleared of red cells and granulocytes by centrifugation over Ficoll-Hypaque were cryopreserved at 1 degree C/min in 10% Me2SO and stored at -150 degrees C. Cryopreserved cells were thawed rapidly, diluted at a constant rate over 10 min with 9 vol of media, and washed twice prior to study. Antibody-dependent cell-mediated cytotoxicity (ADCC) activity against anti-D-coated Rh-positive erythrocytes of both fresh and cryopreserved PBM was tested and found to be equal (52.5 vs 51%). The myeloperoxidase positive, EA-rosette-positive population in cryopreserved cells was 39% compared with 17% for fresh cells (P less than 0.0001). This difference is due to preferential recovery of cryopreserved monocytes among mononuclear cells. The proportion of cells expressing Fc receptors among the myeloperoxidase-positive mononuclear cell population increased after freezing, suggesting an alteration in membrane structure induced by cryopreservation. It is concluded that PBM can be cryopreserved in Me2SO and that ADCC function is fully retained in the cryopreserved cells. This study along with a previous study (R.S. Weiner and S.J. Norman, J. Natl. Cancer Inst. 66, 255-260, 1981) demonstrate the feasibility of using cryopreserved human PBM for functional studies.

摘要

人类外周血单核细胞(PBM)调节并参与多种宿主防御反应。PBM的冷冻保存有助于对其功能进行研究。通过在Ficoll-Hypaque上离心去除红细胞和粒细胞后的外周血样本,在10%二甲基亚砜(Me2SO)中以1℃/分钟的速度冷冻保存,并储存在-150℃。冷冻保存的细胞迅速解冻,在10分钟内以恒定速率用9倍体积的培养基稀释,并在研究前洗涤两次。测试了新鲜和冷冻保存的PBM对包被抗-D的Rh阳性红细胞的抗体依赖性细胞介导的细胞毒性(ADCC)活性,发现二者相等(分别为52.5%和51%)。冷冻保存细胞中髓过氧化物酶阳性、EA花环阳性的群体为39%,而新鲜细胞为17%(P<0.0001)。这种差异是由于冷冻保存的单核细胞在单核细胞中优先恢复。冷冻后,髓过氧化物酶阳性单核细胞群体中表达Fc受体的细胞比例增加,提示冷冻保存诱导了膜结构的改变。结论是PBM可以在Me2SO中冷冻保存,且冷冻保存的细胞中ADCC功能完全保留。本研究与之前的一项研究(R.S.韦纳和S.J.诺曼,《国家癌症研究所杂志》66卷,255 - 260页,1981年)证明了使用冷冻保存的人类PBM进行功能研究的可行性。

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