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C3d,g存在于正常人类表皮基底膜中。

C3d,g is present in normal human epidermal basement membrane.

作者信息

Basset-Seguin N, Dersookian M, Cehrs K, Yancey K B

机构信息

Department of Dermatology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.

出版信息

J Immunol. 1988 Aug 15;141(4):1273-80.

PMID:3135326
Abstract

mAb as well as polyclonal anti-human C3d antibodies were found to specifically bind to the epidermal basement membrane zone of normal human adult and neonatal skin in a linear continuous pattern on direct immunofluorescence microscopy. No such binding was found in dermal microvascular basement membranes. Studies of normal adult human skin using a rat mAb specific for C3g revealed the same pattern of epidermal basement membrane staining. Control polyclonal antibodies directed against C3, C3c, C5, IgG, IgA, or IgM showed no evidence of epidermal basement membrane binding or in situ deposits of immune complexes in samples of normal human skin that were all positive for C3d and C3g. Pre-adsorption of monoclonal or polyclonal anti-human C3d with purified human C3d completely blocked these reagents' epidermal basement membrane reactivity. Anti-human C3d epidermal basement membrane binding was not diminished by pre-treatment of substrate with antibodies directed against C3, C3c, C5, laminin, fibronectin, or type IV collagen as well as bullous pemphigoid, KF-1, or epidermolysis bullosa acquisita Ag. Direct immunofluorescence microscopy studies on 1 M NaCl split human skin showed that C3d and C3g were found in the base of the cleavage plane created within the lamina lucida. By immunoelectron microscopy, C3d was found along the base of the lamina densa and in the sublamina densa region of normal human epidermal basement membrane. Although anti-human C3d epidermal basement membrane binding was not altered by treatment of 6 micron skin sections with buffers of varying pH and ionic concentration, binding was abolished by treating dermal portions of salt split skin with 0.1 M dithiothreitol in 8 M urea. Studies of a patient with congenital C3 deficiency revealed that there was no binding of anti-human C3d or anti-human C3g to this subject's epidermal basement membrane. Moreover, treatment of this patient's skin with aged human serum containing C3d,g or purified human C3 did not restore epidermal basement membrane anti-human C3d binding. These studies demonstrate that C3d,g or a closely related C3 fragment is present in the epidermal basement membrane zone of normal human skin.

摘要

在直接免疫荧光显微镜检查中发现,单克隆抗体以及多克隆抗人C3d抗体能以线性连续模式特异性结合正常成人及新生儿皮肤的表皮基底膜带。在真皮微血管基底膜中未发现此类结合。使用对C3g特异的大鼠单克隆抗体对正常成人皮肤进行研究,显示出相同的表皮基底膜染色模式。针对C3、C3c、C5、IgG、IgA或IgM的对照多克隆抗体,在所有C3d和C3g均为阳性的正常人皮肤样本中,未显示出表皮基底膜结合或免疫复合物原位沉积的证据。用纯化的人C3d对单克隆或多克隆抗人C3d进行预吸附,完全阻断了这些试剂与表皮基底膜的反应性。用针对C3、C3c、C5、层粘连蛋白、纤连蛋白或IV型胶原以及大疱性类天疱疮、KF-1或获得性大疱性表皮松解症抗原的抗体对底物进行预处理,抗人C3d与表皮基底膜的结合并未减弱。对1M NaCl分离的人皮肤进行直接免疫荧光显微镜研究表明,在透明层内形成的分裂平面底部发现了C3d和C3g。通过免疫电子显微镜检查,在正常人表皮基底膜的致密层底部和致密层下区域发现了C3d。尽管用不同pH和离子浓度的缓冲液处理6微米皮肤切片不会改变抗人C3d与表皮基底膜的结合,但用8M尿素中的0.1M二硫苏糖醇处理盐分离皮肤的真皮部分会消除结合。对一名先天性C3缺乏症患者的研究表明,抗人C3d或抗人C3g与该患者的表皮基底膜无结合。此外,用含有C3d、g的老化人血清或纯化的人C3处理该患者的皮肤,并未恢复表皮基底膜抗人C3d的结合。这些研究表明,C3d、g或与之密切相关的C3片段存在于正常人皮肤的表皮基底膜带中。

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