首页> 美国卫生研究院文献>Biochemical Journal >Immunocomplexes stimulate different signalling events to chemoattractants in the neutrophil and regulate L-selectin and beta 2-integrin expression differently.
【2h】

Immunocomplexes stimulate different signalling events to chemoattractants in the neutrophil and regulate L-selectin and beta 2-integrin expression differently.

机译:免疫复合物刺激嗜中性粒细胞趋化因子的不同信号传递事件并不同地调节L-选择蛋白和β2-整合素的表达。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Neutrophils express receptors for numerous phlogistons which, when occupied, trigger distinct signal-transduction pathways. Previous studies have shown that stimulation of neutrophils with chemoattractants induces shedding of the adhesive molecule L-selectin and increased expression of the beta 2-integrin CD11b/CD18. We determined the effect of ligation of classic, G-protein-linked chemoattractant receptors [C5a, interleukin-8 (IL-8), formylmethionyl-leucylphenylalanine (FMLP) and substance P], receptors for the Fc portion of IgG (Fc gamma receptors) and receptors for transforming growth factor beta (TGF beta) on expression of adhesive molecules by neutrophils and the stimulus-transduction mechanisms thought to mediate these changes. We were surprised to observe that occupancy of Fc gamma receptors by immunocomplexes (BSA-anti-BSA) stimulated increased expression by neutrophils of CD11b/CD18 at concentrations which did not affect L-selectin expression (EC50 9 micrograms/ml versus 350 micrograms/ml respectively, P < 0.00001, n = 5). In contrast, similar to previous studies, recombinant C5a, recombinant IL-8 and FMLP all stimulated increased expression of CD11b/CD18 (170-260% of basal, P < 0.001, n = 5) and shedding of L-selectin (56-75% reduction from basal, P < 0.001, n = 5) at similar concentrations and with similar potencies (EC50 = 2, 5, and 3 nM respectively). In contrast, neither TGF beta 1 nor, surprisingly, substance P affected expression of CD11b/CD18 or L-selectin. The regulation of expression of CD11b/CD18 or L-selectin in response to FMLP or immunocomplexes was unaffected by cytochalasin B (5 micrograms/ml) or the tyrosine kinase inhibitor tyrphostin-25 (25 microM). Although occupancy of both chemoattractant (FMLP) and Fc gamma receptors stimulated increments in the second messenger diacylglycerol, disruption of actin microfilaments by cytochalasin B enhanced diacylglycerol generation in response to FMLP but not in response to ligation of Fc gamma receptors. Moreover, both FMLP and immune aggregates provoked fluxes of intracellular Ca2+ concentration which differed with respect to both magnitude and kinetics and did not correlate well with regulation of adhesive-molecule expression. As upregulation of CD11b/CD18 is tightly linked to exocytosis of specific granules, these results suggest that shedding of L-selectin by activated neutrophils is not linked to exocytosis. These studies provide further evidence that receptors for chemoattractants and immunocomplexes on the neutrophil are linked to multiple signalling pathways.
机译:中性粒细胞表达多种发色团的受体,这些受体被占领后会触发不同的信号转导途径。先前的研究表明,用化学吸引剂刺激嗜中性粒细胞可诱导粘附分子L-选择蛋白脱落,并增加β2-整合素CD11b / CD18的表达。我们确定了经典的G蛋白连接的趋化因子受体[C5a,白介素8(IL-8),甲酰基甲硫基-亮氨酰苯丙氨酸(FMLP)和P物质],IgG Fc部分的受体(Fcγ受体)的连接作用。 )和中性粒细胞在粘附分子表达时转化生长因子β(TGFβ)的受体,以及认为介导这些变化的刺激转导机制。我们惊讶地发现免疫复合物(BSA-anti-BSA)对Fcγ受体的占用会在不影响L-选择素表达的浓度(EC50为9微克/毫升,而对350微克/毫升为浓度)的情况下刺激中性粒细胞CD11b / CD18的表达增加分别为P <0.00001,n = 5)。相反,类似于先前的研究,重组C5a,重组IL-8和FMLP均刺激CD11b / CD18表达增加(基础的170-260%,P <0.001,n = 5)和L-选择素的脱落(56-在相似的浓度和相似的效价下(EC50分别为2、5和3 nM)从基础减少75%,P <0.001,n = 5)。相反,TGF beta 1和P物质都不会影响CD11b / CD18或L-选择蛋白的表达。响应于FMLP或免疫复合物的CD11b / CD18或L-选择素的表达调控不受细胞松弛素B(5微克/毫升)或酪氨酸激酶抑制剂tyrphostin-25(25微摩尔)的影响。尽管同时存在化学吸引剂(FMLP)和Fcγ受体会刺激第二信使二酰基甘油的增加,但细胞松弛素B对肌动蛋白微丝的破坏会增强二酰基甘油的生成,以响应FMLP,而不是响应Fcγ受体的连接。而且,FMLP和免疫聚集体均会引起细胞内Ca2 +浓度的通量,这些通量在大小和动力学方面均不同,并且与粘附分子表达的调控关系不大。由于CD11b / CD18的上调与特定颗粒的胞吐作用紧密相关,因此这些结果表明,活化嗜中性粒细胞释放L-选择蛋白与胞吐作用无关。这些研究提供了进一步的证据,表明嗜中性粒细胞上趋化因子和免疫复合物的受体与多种信号通路相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号