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淋巴细胞功能相关抗原-1和细胞间黏附分子-1在破骨细胞生成中的作用:在破骨细胞前体之间直接相互作用中的可能作用。

Involvement of lymphocyte function-associated antigen-1 and intercellular adhesion molecule-1 in osteoclastogenesis: a possible role in direct interaction between osteoclast precursors.

作者信息

Harada H, Kukita T, Kukita A, Iwamoto Y, Iijima T

机构信息

Second Department of Oral Anatomy, Faculty of Dentistry, Kyushu University, Fukuoka, Japan.

出版信息

Endocrinology. 1998 Sep;139(9):3967-75. doi: 10.1210/endo.139.9.6171.

Abstract

In our search for molecules involved in the process of osteoclast differentiation, we examined the surface phenotypes of the preosteoclast-like cells and osteoclast-like multinucleated cells (MNCs) formed in bone marrow cultures, using monoclonal antibodies recognizing different antigen molecules expressed on hematopoietic cells. Among these cell surface antigens, lymphocyte function-associated antigen-1 (LFA-1) and intercellular adhesion molecule-1 (ICAM-1) were highly expressed on mononuclear cells in the cultures for forming preosteoclast-like mononuclear cells. The double detection of these two antigen molecules with osteoclast-specific antigen and with calcitonin receptor, using a fluorescence-activated cell sorter or autoradiography technique, revealed that LFA-1 and ICAM-1 were expressed on the preosteoclasts. The expression of ICAM-1 was detected on both preosteoclasts and osteoclast-like MNCs, whereas the expression of LFA-1 was restricted to preosteoclasts. We designed a peptide with the sequence of the binding site of ICAM-1 against the ligand LFA-1. In the whole bone marrow culture system for forming osteoclast-like MNCs, a significant inhibition of MNC formation was observed by the addition of this peptide. These results strongly suggest the involvement of an LFA-1/ICAM-1-interaction in osteoclastogenesis.

摘要

在寻找参与破骨细胞分化过程的分子时,我们使用识别造血细胞上表达的不同抗原分子的单克隆抗体,检测了骨髓培养物中形成的前破骨细胞样细胞和破骨细胞样多核细胞(MNCs)的表面表型。在这些细胞表面抗原中,淋巴细胞功能相关抗原-1(LFA-1)和细胞间黏附分子-1(ICAM-1)在用于形成前破骨细胞样单核细胞的培养物中的单核细胞上高度表达。使用荧光激活细胞分选仪或放射自显影技术,将这两种抗原分子与破骨细胞特异性抗原和降钙素受体进行双重检测,结果显示LFA-1和ICAM-1在前破骨细胞上表达。ICAM-1在前破骨细胞和破骨细胞样MNCs上均有表达,而LFA-1的表达仅限于前破骨细胞。我们设计了一种具有ICAM-1与配体LFA-1结合位点序列的肽。在用于形成破骨细胞样MNCs的全骨髓培养系统中,添加该肽后观察到MNC形成受到显著抑制。这些结果强烈表明LFA-1/ICAM-1相互作用参与了破骨细胞生成。

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