Hart Simon P, Alexander Karen M, MacCall Shonna M, Dransfield Ian
MRC Centre for Inflammation Research, University of Edinburgh Medical School, Teviot Place, Edinburgh EH8 9AG, UK.
J Inflamm (Lond). 2005 May 31;2:5. doi: 10.1186/1476-9255-2-5.
It has been reported that C-reactive protein (CRP) binds both leukocyte FcgammaRIIA (CD32) and the plasma membrane of apoptotic cells. Since FcgammaRIIA becomes functionally enabled during neutrophil apoptosis, we sought to determine whether CRP bound to apoptotic neutrophils via FcgammaRIIA.
We prepared directly labelled CRP and demonstrated that it was essentially free of IgG. We looked for evidence of CRP binding to intact, membrane impermeable apoptotic human neutrophils and to FcgammaRIIA-transfected Jurkat cells. We examined the functional consequences of incubation with CRP upon phagocytosis of apoptotic cells by human monocyte-derived macrophages.
We could not detect binding of purified soluble CRP to classical early apoptotic human neutrophils or to FcgammaRIIA-transfected Jurkat cells. In contrast, membrane-permeable late apoptotic neutrophils exhibited strong CRP binding, which comprised both Ca2+-dependent and heparin-inhibitable Ca2+-independent components. However, there was no effect of CRP binding upon phagocytosis of late apoptotic neutrophils by macrophages.
Potential apoptotic cell opsonins such as CRP may bind only to intracellular structures in cells with leaky membranes that have progressed to a late stage of apoptosis.
据报道,C反应蛋白(CRP)可与白细胞FcγRIIA(CD32)及凋亡细胞的质膜结合。由于FcγRIIA在中性粒细胞凋亡过程中功能得以激活,我们试图确定CRP是否通过FcγRIIA与凋亡中性粒细胞结合。
我们制备了直接标记的CRP,并证明其基本不含IgG。我们寻找CRP与完整的、膜不可渗透的凋亡人中性粒细胞以及FcγRIIA转染的Jurkat细胞结合的证据。我们研究了与CRP孵育对人单核细胞衍生巨噬细胞吞噬凋亡细胞的功能影响。
我们未检测到纯化的可溶性CRP与典型的早期凋亡人中性粒细胞或FcγRIIA转染的Jurkat细胞结合。相反,膜可渗透的晚期凋亡中性粒细胞表现出强烈的CRP结合,其包括Ca2+依赖和肝素抑制的Ca2+非依赖成分。然而,CRP结合对巨噬细胞吞噬晚期凋亡中性粒细胞没有影响。
潜在的凋亡细胞调理素如CRP可能仅与已进展至凋亡晚期且膜有渗漏的细胞内结构结合。