Kzhyshkowska Julia
Department of Dermatology, University Medical Centre Mannheim, Ruprecht-Karls University of Heidelberg, Mannheim, Germany.
ScientificWorldJournal. 2010 Oct 12;10:2039-53. doi: 10.1100/tsw.2010.189.
The multifunctional scavenger receptor stabilin-1 (STAB1, FEEL-1, CLEVER-1, KIAA0246) is expressed on tissue macrophages and sinusoidal endothelial cells in healthy organisms, and its expression on both macrophages and different subtypes of endothelial cells is induced during chronic inflammation and tumor progression. Stabilin-1 is a type-1 transmembrane receptor that mediates endocytic and phagocytic clearance of "unwanted-self" components, intracellular sorting of the endogenously synthesized chitinase-like protein SI-CLP, and transcytosis of the growth hormone family member placental lactogen. The central sorting station for stabilin-1 trafficking seems to be the trans-Golgi network (TGN). Transport of stabilin-1 in the TGN requires interaction with GGA adaptors that bind to the classical DDSLL motif and a novel acidic cluster in its cytoplasmic tail. Degradation of stabilin-1 seems to depend on the interaction with sorting nexin 17. However, the mechanisms keeping stabilin-1 on the cell surface remain to be identified. This issue deserves specific attention due to the growing amount of data indicating that function of stabilin-1 in cell adhesion events is essential for inflammation and metastasis. Taking into consideration the complexity of stabilin-1-mediated processes, investigation of stabilin-1 functions in the animal models, as well as mathematic modeling of intracellular trafficking and extracellular contact, would enable prediction of stabilin-1 behavior in complex biological systems and would open perspectives for therapeutic targeting of stabilin-1 pathways in chronic inflammation and carcinogenesis.
多功能清道夫受体稳定素-1(STAB1、FEEL-1、CLEVER-1、KIAA0246)在健康生物体的组织巨噬细胞和窦状内皮细胞上表达,并且在慢性炎症和肿瘤进展过程中,其在巨噬细胞和不同亚型内皮细胞上的表达均被诱导。稳定素-1是一种1型跨膜受体,介导“非自身”成分的内吞和吞噬清除、内源性合成的几丁质酶样蛋白SI-CLP的细胞内分选以及生长激素家族成员胎盘催乳素的转胞吞作用。稳定素-1转运的中心分选站似乎是反式高尔基体网络(TGN)。稳定素-1在TGN中的运输需要与结合到其细胞质尾部经典DDSLL基序和一个新的酸性簇的GGA衔接蛋白相互作用。稳定素-1的降解似乎取决于与分选连接蛋白17的相互作用。然而,使稳定素-1保留在细胞表面的机制仍有待确定。鉴于越来越多的数据表明稳定素-1在细胞黏附事件中的功能对炎症和转移至关重要,这个问题值得特别关注。考虑到稳定素-1介导过程的复杂性,在动物模型中研究稳定素-1的功能,以及对细胞内运输和细胞外接触进行数学建模,将能够预测稳定素-1在复杂生物系统中的行为,并为慢性炎症和致癌过程中稳定素-1途径的治疗靶向开辟前景。