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一种从人外周血单核细胞中产生并测定组胺释放活性的方法。

A method for production and determination of histamine releasing activity from human peripheral blood mononuclear cells.

作者信息

Kampen G T, Poulsen L K, Reimert C M, Skov P S

机构信息

Laboratory of Medical Allergology, Allergy Unit, RHIMA 7542, National University Hospital, Copenhagen, Denmark.

出版信息

J Immunol Methods. 1997 Dec 29;210(2):185-93. doi: 10.1016/s0022-1759(97)00187-7.

Abstract

Histamine releasing factors, i.e. cytokines capable of inducing histamine release from basophils or mast cells, have been suggested to be involved in the pathogenesis of, for example, allergic late-phase reactions. Here we describe a controlled method for production and determination of histamine releasing activity (HRA) from human peripheral blood mononuclear cells (MNC). MNC were incubated with concanavalin A (Con A) for 2 h and cultured for another 40 h in fresh serum free medium. The culture supernatants were concentrated 19-25 fold by ultrafiltration (molecular weight cut-off: 3000 Da). The preparations of HRA induced dose- and Ca2+-dependent histamine release from leukocytes. Supernatants of parallel cultures of unstimulated MNC did not induce histamine release. The HRA was neither due to exogenous histamine releasing compounds (e.g. Con A) nor to residual histamine in the preparations of HRA. The kinetics of HRA induced histamine release (half-maximal release after > 40 min) were slower and more protracted than those of anti-IgE induced histamine release. However, based on a comparison between HRA induced histamine release from leukocytes and purified (97%) basophils, this did not appear to be due to an indirect effect on the basophils. Finally, neither the production of nor the response to HRA was dependent on the allergic status of the donor.

摘要

组胺释放因子,即能够诱导嗜碱性粒细胞或肥大细胞释放组胺的细胞因子,被认为参与了例如过敏性迟发相反应的发病机制。在此,我们描述了一种用于从人外周血单个核细胞(MNC)产生并测定组胺释放活性(HRA)的可控方法。将MNC与伴刀豆球蛋白A(Con A)孵育2小时,然后在新鲜无血清培养基中再培养40小时。通过超滤(截留分子量:3000 Da)将培养上清液浓缩19 - 25倍。HRA制剂可诱导白细胞呈剂量和Ca2+依赖性释放组胺。未刺激的MNC平行培养物的上清液不诱导组胺释放。HRA既不是由于外源性组胺释放化合物(如Con A),也不是由于HRA制剂中的残留组胺。HRA诱导组胺释放的动力学(> 40分钟后达到最大释放量的一半)比抗IgE诱导组胺释放的动力学更缓慢且更持久。然而,基于对HRA诱导白细胞和纯化(97%)嗜碱性粒细胞释放组胺的比较,这似乎并非对嗜碱性粒细胞的间接作用所致。最后,HRA的产生及对HRA的反应均不依赖于供体的过敏状态。

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