人肥大细胞在棕榈黄斑形成中的可能作用。

IF 2.5 4区 医学 Q2 PATHOLOGY Pathology International Pub Date : 2023-09-01 DOI:10.1111/pin.13347
Hiroya Nakamura, Takashi Matsuzaki, Ken R Ito, Ryota Nakagawa, Lurica M Asano, Hinako Nishikido, Hironori Haga, Tatsuki R Kataoka
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引用次数: 0

摘要

皮肤黄瘤由起源于单核细胞或巨噬细胞的泡沫细胞组成,积聚在皮肤的血管周围区域。这些细胞的主要成分是氧化低密度脂蛋白(oxLDL)。在这项研究中,我们发现肥大细胞包围了积聚的泡沫细胞,表明它们参与了黄瘤的形成。THP-1或U937单核细胞与人肥大细胞系LUVA共培养可上调它们对oxLDL的摄取。在最常见的皮肤黄瘤、palpebrarum黄斑瘤和共培养的病理标本中,肥大细胞和泡沫细胞之间的细胞内细胞粘附分子-1 (ICAM-1)染色呈阳性。在后者中,ICAM1信使RNA水平上调。抗icam -1阻断抗体抑制THP-1或U937单核细胞与LUVA共培养对oxLDL摄取的增加。综上所述,这些结果表明肥大细胞在棕榈黄斑形成中的作用以及ICAM-1在这一过程中的参与。
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Possible roles of human mast cells in the formation of xanthelasma palpebrarum.

Cutaneous xanthoma consist of foam cells that originate from monocytes or macrophages and accumulate in perivascular areas of the skin. The main component of these cells is oxidized low-density lipoprotein (oxLDL). In this study, we show that mast cells surround the accumulated foam cells, suggesting their involvement in xanthoma formation. Coculture of THP-1 or U937 monocytes with the human mast cell line LUVA upregulated their uptake of oxLDL. Positive staining for intracellular cell adhesion molecule-1 (ICAM-1) at the borders between mast cells and foam cells was seen in pathological specimens of the most common cutaneous xanthoma, xanthelasma palpebrarum, and in cocultures. In the latter, ICAM1 messenger RNA levels were upregulated. The administration of anti-ICAM-1 blocking antibody inhibited the increase in oxLDL uptake by THP-1 or U937 monocytes cocultured with LUVA. Taken together, these results suggest a role for mast cells in the formation of xanthelasma palpebrarum and the involvement of ICAM-1 in this process.

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来源期刊
Pathology International
Pathology International 医学-病理学
CiteScore
4.50
自引率
4.50%
发文量
102
审稿时长
12 months
期刊介绍: Pathology International is the official English journal of the Japanese Society of Pathology, publishing articles of excellence in human and experimental pathology. The Journal focuses on the morphological study of the disease process and/or mechanisms. For human pathology, morphological investigation receives priority but manuscripts describing the result of any ancillary methods (cellular, chemical, immunological and molecular biological) that complement the morphology are accepted. Manuscript on experimental pathology that approach pathologenesis or mechanisms of disease processes are expected to report on the data obtained from models using cellular, biochemical, molecular biological, animal, immunological or other methods in conjunction with morphology. Manuscripts that report data on laboratory medicine (clinical pathology) without significant morphological contribution are not accepted.
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