首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Mannose Receptor and Its Putative Ligands in Normal Murine Lymphoid and Nonlymphoid Organs: In Situ Expression of Mannose Receptor by Selected Macrophages Endothelial Cells Perivascular Microglia and Mesangial Cells but not Dendritic Cells
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Mannose Receptor and Its Putative Ligands in Normal Murine Lymphoid and Nonlymphoid Organs: In Situ Expression of Mannose Receptor by Selected Macrophages Endothelial Cells Perivascular Microglia and Mesangial Cells but not Dendritic Cells

机译:正常小鼠淋巴和非淋巴器官中的甘露糖受体及其推定配体:所选巨噬细胞内皮细胞血管周围小胶质细胞和系膜细胞但不是树突状细胞的甘露糖受体的原位表达。

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摘要

The mannose receptor (MR) has established roles in macrophage (Mφ) phagocytosis of microorganisms and endocytic clearance of host-derived glycoproteins, and has recently been implicated in antigen capture by dendritic cells (DCs) in vitro. MR is the founder member of a family of homologous proteins, and its recognition properties differ according to its tissue of origin. Given this heterogeneity and our recent discovery of a soluble form of MR in mouse serum, we studied the sites of synthesis of MR mRNA and expression of MR protein in normal mouse tissues. We demonstrate that synthesis and expression occur at identical sites, and that mature Mφ and endothelium are heterogeneous with respect to MR expression, additionally describing MR on perivascular microglia and glomerular mesangial cells. However, MR was not detected on DCs in situ, or on marginal zone or subcapsular sinus Mφ, both of which have MR-like binding activities. We also compared expression of MR to the binding of a recombinant probe containing the cysteine-rich domain of MR. We show that MR and its putative ligand(s) are expressed at nonoverlapping sites within lymphoid organs, consistent with a transfer function for soluble MR. Therefore, in addition to endocytic and phagocytic roles, MR may play an important role in antigen recognition and transport within lymphoid organs.
机译:甘露糖受体(MR)在微生物的巨噬细胞(Mφ)吞噬作用和宿主衍生的糖蛋白的内吞清除中已建立作用,并且最近涉及体外树突状细胞(DC)的抗原捕获。 MR是同源蛋白家族的创始成员,其识别特性因其来源组织而异。鉴于这种异质性,以及我们最近在小鼠血清中发现MR的可溶形式,我们研究了MR mRNA的合成位点和MR蛋白在正常小鼠组织中的表达。我们证明了合成和表达发生在相同的位置,并且成熟的Mφ和内皮相对于MR表达而言是异质的,另外还描述了血管周小胶质细胞和肾小球系膜细胞上的MR。但是,未在原位DC或边缘区或囊下窦Mφ上检测到MR,这两者均具有MR样结合活性。我们还比较了MR的表达与包含MR富含半胱氨酸结构域的重组探针的结合。我们显示,MR及其推定的配体在淋巴器官内的非重叠位点表达,与可溶性MR的传递功能一致。因此,除了内吞和吞噬作用,MR可能在淋巴器官内的抗原识别和转运中起重要作用。

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