CD151: Basis Sequence: Mouse.
CD151: Basis Sequence: Mouse.
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CD151:基础序列:小鼠。
DOI:
10.1038/mp.a004123.01
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发表时间:
2011
期刊:
影响因子:
--
通讯作者:
Zijlstra,Andries
中科院分区:
文献类型:
--
作者:
Palmer,TrenisD;Zijlstra,Andries
CD151 is a member of the Tetraspanin (Tspan) family of transmembrane proteins, which encompasses 33 members in mammals, including CD9 (MRP1), CD63 (LAMP3), CD81 (TAPA1), and CD82 (Kai1). All members of this family possess a common structure containing four membrane-spanning domains arranged in a compact rod-like fashion (Hemler 2005), which leads to the formation of the large and small extracellular loops (LEL and SEL respectively). CD151 functions principally as a transmembrane scaffolding protein. Like most Tspans, CD151 interacts with other transmembrane or membrane-proximal proteins through its LEL and short cytoplasmic tails. Multimerization of the Tspan and its partner proteins leads to the formation of large multimolecular complexes within the membrane. These complexes were originally referred to as the ‘tetraspanin web’(Charrin et al. 2003; Kovalenko et al. 2004; Levy and Shoham 2005); however, the most current literature refers to them as tetraspanin-enriched microdomains (TERMs or TEM; Hemler 2008; Zöller 2009). The LEL contains the majority of amino acids important for interactions with transmembrane and membrane-proximal partners, while the transmembrane regions and cytoplasmic tails are thought to be required for intracellular interactions with Tspanassociated cytoplasmic signaling molecules. Specific partners include integrins α3β1 and α6β4, phosphatidylinositol 4-kinase (PI4 kinase) and protein kinase C α (PKCα). The molecular mechanism (s) by which this Tspan conveys biological activity remains under investigation. CD151 participates in a wide variety of normal physiological processes as well as pathologies, including kidney function, angiogenesis, platelet activation, inflammation, wound healing, tumor invasion, and metastasis (Hemler et al. 2003; Lau et al. 2004; Kolesnikova et al. 2004; Cowin et al. 2006; Sachs et al. 2006; Sterk et al. 2000; Stipp and Hemler 2000; Takeda et al. 2007; Wright et al. 2004; Yáñez-Mó et al. 2008; Zijlstra et al. 2008).