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人类CD44胞外域的N端和中央区域参与细胞表面透明质酸的结合。

N-terminal and central regions of the human CD44 extracellular domain participate in cell surface hyaluronan binding.

作者信息

Liao H X, Lee D M, Levesque M C, Haynes B F

机构信息

Department of Medicine, Duke Arthritis Center, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

J Immunol. 1995 Oct 15;155(8):3938-45.

PMID:7561101
Abstract

CD44 molecules are cell surface receptors for hyaluronan (HA). To define regions of the extracellular domain of CD44 that are important for HA binding, we have studied the ability of HA-blocking CD44 mAbs to bind to CD44 from a variety of sources. Five CD44 mAbs (5F12, BRIC235, 3F12, BU-75, and HP2/9) of 21 studied were identified that at least partially blocked FITC-labeled HA (HA-FITC) binding to the standard form of CD44 (CD44S) in CD44-transfected Jurkat cells. Analysis of reactivity of HA-blocking CD44 mAbs defined three distinct epitopes. Lack of reactivity of mAb 5F12 with a CD44 fusion protein (CD44-Rg) containing an N-terminal truncation of 20 amino acids (aa), as well as reactivity of mAb 5F12 with an N-terminal CD44 synthetic peptide (CD44-9A), demonstrated that the N-terminal proximal region of CD44 (aa 1 to 20) was involved in mAb 5F12 binding. A mutant cell line, CEM-NKR, derived from the T-ALL cell line, CEM, did not bind mAb 5F12 nor bind HA, whereas wild-type CEM did bind mAb 5F12 and HA. Sequence analysis of wild-type CEM and CEM-NKR CD44 cDNA demonstrated a G to A point mutation at position 575 in the CD44 cDNA of CEM-NKR, resulting in an arginine to histidine mutation at aa position 154. Taken together, our studies demonstrated that there are three epitopes to which HA-blocking mAbs bind in the extracellular domain of CD44, and that the CD44 N-terminal proximal and central regions are two regions in the extracellular domain of CD44 that may interact and either mediate or regulate HA binding to cell surface CD44.

摘要

CD44分子是透明质酸(HA)的细胞表面受体。为了确定CD44细胞外结构域中对HA结合至关重要的区域,我们研究了HA阻断性CD44单克隆抗体与多种来源的CD44结合的能力。在所研究的21种CD44单克隆抗体中,鉴定出5种(5F12、BRIC235、3F12、BU - 75和HP2/9)至少部分阻断了异硫氰酸荧光素标记的HA(HA - FITC)与CD44转染的Jurkat细胞中标准形式的CD44(CD44S)的结合。对HA阻断性CD44单克隆抗体反应性的分析确定了三个不同的表位。单克隆抗体5F12与含有20个氨基酸(aa)N端截短的CD44融合蛋白(CD44 - Rg)无反应性,以及单克隆抗体5F12与N端CD44合成肽(CD44 - 9A)有反应性,表明CD44的N端近端区域(aa 1至20)参与了单克隆抗体5F12的结合。一种源自T - ALL细胞系CEM的突变细胞系CEM - NKR,既不结合单克隆抗体5F12也不结合HA,而野生型CEM确实结合单克隆抗体5F12和HA。野生型CEM和CEM - NKR CD44 cDNA的序列分析表明,CEM - NKR的CD44 cDNA中第575位存在G到A的点突变,导致aa位置154处精氨酸到组氨酸的突变。综上所述,我们的研究表明,在CD44的细胞外结构域中有三个HA阻断性单克隆抗体结合的表位,并且CD44的N端近端和中央区域是CD44细胞外结构域中可能相互作用并介导或调节HA与细胞表面CD44结合的两个区域。

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