Daggett M A, Li Q, Weaver R F, Suprenant K A
Department of Biochemistry, Cell and Molecular Biology, University of Kansas, Lawrence 66045, USA.
Cell Motil Cytoskeleton. 1998;41(1):57-67. doi: 10.1002/(SICI)1097-0169(1998)41:1<57::AID-CM5>3.0.CO;2-C.
The purpose of this study was to test whether any assembly-promoting microtubule-associated protein (MAP) would bundle microtubules and induce process formation in recombinant baculovirus-infected Sf9 cells, in particular, whether a non-neural MAP from a normally rounded cell would produce cellular asymmetries. To carry out these experiments, we constructed a recombinant baculovirus that expressed the full-length 77-kD EMAP, an abundant MAP that localizes to the mitotic spindle of cleavage-stage sea urchin embryos and to the interphase array of microtubules in adult coelomocytes. Expression of EMAP in Sf9 cells had no detectable effect on cellular morphology, microtubule organization, or stability. These results indicate that process formation in Sf9 cells is MAP specific.
本研究的目的是测试是否有任何促进组装的微管相关蛋白(MAP)能在重组杆状病毒感染的Sf9细胞中使微管成束并诱导突起形成,特别是来自正常圆形细胞的非神经MAP是否会产生细胞不对称性。为了进行这些实验,我们构建了一种表达全长77-kD EMAP的重组杆状病毒,EMAP是一种丰富的MAP,定位于卵裂期海胆胚胎的有丝分裂纺锤体以及成年体腔细胞的微管间期阵列。EMAP在Sf9细胞中的表达对细胞形态、微管组织或稳定性没有可检测到的影响。这些结果表明,Sf9细胞中的突起形成具有MAP特异性。