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硬皮病中皮肤细胞浸润的超微结构

Ultrastructure of cutaneous cellular infiltrates in scleroderma.

作者信息

Fleischmajer R, Perlish J S, West W P

出版信息

Arch Dermatol. 1977 Dec;113(12):1661-6.

PMID:202203
Abstract

Electron microscopy of the skin was performed in ten patients with systemic and four with localized scleroderma. The following three groups of cells were identified: (1) mature lymphocytes, T lymphoblasts, immature plasma cells, and plasma cells; (2) fibroblasts, fibrocytes, and fibroblast-like cells; and (3) macrophages, undifferentiated mesenchymal cells, and monocytes. Inthose specimens with mononuclear cell infiltrates, the most common cells were lymphocytic-types, macrophages, and fibroblasts with well developed rough endoplasmic reticulum. In the specimens at the fibrotic stage, fibroblasts and histiocytic-type cells predominated. This study suggests that cellular and humoral immunity may play a role in the pathophysiology of scleroderma.

摘要

对10例系统性硬皮病患者和4例局限性硬皮病患者的皮肤进行了电子显微镜检查。识别出以下三组细胞:(1)成熟淋巴细胞、T淋巴母细胞、未成熟浆细胞和浆细胞;(2)成纤维细胞、纤维细胞和成纤维样细胞;(3)巨噬细胞、未分化间充质细胞和单核细胞。在有单核细胞浸润的标本中,最常见的细胞是淋巴细胞类型、巨噬细胞和成纤维细胞,其粗面内质网发达。在纤维化阶段的标本中,成纤维细胞和组织细胞类型的细胞占主导。这项研究表明,细胞免疫和体液免疫可能在硬皮病的病理生理学中起作用。

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1
Ultrastructure of cutaneous cellular infiltrates in scleroderma.硬皮病中皮肤细胞浸润的超微结构
Arch Dermatol. 1977 Dec;113(12):1661-6.
2
[Increased retraction of collagen lattices by fibroblasts from patients with scleroderma].[硬皮病患者成纤维细胞对胶原晶格回缩增加]
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H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases.H综合征:一种近期定义的具有独特组织学特征的遗传性皮肤病。10例病例的形态学、组织化学、免疫组织化学及超微结构研究
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Ultrastructure of generalized scleroderma.全身性硬皮病的超微结构
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Antibodies eluted from lymphoid cell membrane. Occurrence in certain varieties of scleroderma.从淋巴细胞膜洗脱的抗体。在某些硬皮病变种中的出现情况。
Arch Dermatol. 1979 Jun;115(6):709-12.

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Clin Transl Med. 2024 Jan;14(1):e1545. doi: 10.1002/ctm2.1545.
2
Molecular and cellular basis of scleroderma.硬皮病的分子与细胞基础
J Mol Med (Berl). 2014 Sep;92(9):913-24. doi: 10.1007/s00109-014-1190-x. Epub 2014 Jul 18.
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Tumor necrosis factor-costimulated T lymphocytes from patients with systemic sclerosis trigger collagen production in fibroblasts.
来自系统性硬化症患者的肿瘤坏死因子共刺激T淋巴细胞可触发成纤维细胞产生胶原蛋白。
Arthritis Rheum. 2013 Feb;65(2):481-91. doi: 10.1002/art.37738.
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Supernatants from culture of type I collagen-stimulated PBMC from patients with cutaneous systemic sclerosis versus localized scleroderma demonstrate suppression of MMP-1 by fibroblasts.来自皮肤弥漫性硬皮病与局限性硬皮病患者的 I 型胶原刺激的 PBMC 培养上清液显示成纤维细胞对 MMP-1 的抑制作用。
Clin Rheumatol. 2012 Jun;31(6):973-81. doi: 10.1007/s10067-012-1962-z. Epub 2012 Feb 25.
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Intrinsic gene expression subsets of diffuse cutaneous systemic sclerosis are stable in serial skin biopsies.弥漫性皮肤系统性硬皮病的内在基因表达亚群在连续皮肤活检中稳定。
J Invest Dermatol. 2012 May;132(5):1363-73. doi: 10.1038/jid.2011.472. Epub 2012 Feb 9.
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Fibrillin assemblies: extracellular determinants of tissue formation and fibrosis.原纤维蛋白组装体:组织形成和纤维化的细胞外决定因素
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Studies on endothelial cell cytotoxic activity in sera of patients with progressive systemic sclerosis, Raynaud syndrome, rheumatoid arthritis, and systemic lupus erythematosus.对进行性系统性硬化症、雷诺综合征、类风湿性关节炎和系统性红斑狼疮患者血清中内皮细胞细胞毒性活性的研究。
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Gamma-interferon inhibits collagen synthesis in vivo in the mouse.γ干扰素在小鼠体内可抑制胶原蛋白的合成。
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