Bose Santanu, Banerjee Amiya K
Department of Virology, The Cleveland Clinic Foundation, Ohio 44195, USA.
Virology. 2002 Jun 20;298(1):73-83. doi: 10.1006/viro.2002.1484.
Our current studies have demonstrated that human parainfluenza virus type 3 (HPIV-3) utilizes heparan sulfate (HS) for its efficient cellular entry. HPIV-3 interacted with HS-agarose in vitro and the cellular entry and infection of HPIV-3 were reduced following (a) infection of human epithelial lung A549 cells with HPIV-3 pre-incubated with soluble HS; (b) treatment of A549 cells with heparinase to remove cell surface HS and sodium chlorate (NaClO(3)), a potent inhibitor of proteoglycan sulfation; and (c) infection of HS-deficient mutant CHO cell lines. However, in each instance, complete inhibition of HPIV-3 entry did not occur, suggesting the presence of additional nonproteoglycan cell surface molecule(s) that is required for HPIV-3 entry. Thus the cell surface HS appears to play an important role in efficient cellular entry of HPIV-3.
我们目前的研究表明,人副流感病毒3型(HPIV-3)利用硫酸乙酰肝素(HS)实现其高效的细胞进入。HPIV-3在体外与HS-琼脂糖相互作用,并且在以下情况下HPIV-3的细胞进入和感染减少:(a)用与可溶性HS预孵育的HPIV-3感染人肺上皮A549细胞;(b)用肝素酶处理A549细胞以去除细胞表面HS和氯酸钠(NaClO₃),一种有效的蛋白聚糖硫酸化抑制剂;以及(c)感染HS缺陷型突变CHO细胞系。然而,在每种情况下,HPIV-3进入并未完全被抑制,这表明存在HPIV-3进入所需的其他非蛋白聚糖细胞表面分子。因此,细胞表面HS似乎在HPIV-3的高效细胞进入中起重要作用。