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Ponticulin plays a role in the positional stabilization of pseudopods.桥粒芯蛋白在伪足的位置稳定中发挥作用。
J Cell Biol. 1995 Dec;131(6 Pt 1):1495-506. doi: 10.1083/jcb.131.6.1495.
2
A Dictyostelium myosin I plays a crucial role in regulating the frequency of pseudopods formed on the substratum.一种盘基网柄菌肌球蛋白I在调节在基质上形成的伪足频率方面起着关键作用。
Cell Motil Cytoskeleton. 1996;33(1):64-79. doi: 10.1002/(SICI)1097-0169(1996)33:1<64::AID-CM7>3.0.CO;2-I.
3
Ponticulin is the major high affinity link between the plasma membrane and the cortical actin network in Dictyostelium.桥粒斑蛋白是盘基网柄菌质膜与皮质肌动蛋白网络之间主要的高亲和力连接物。
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4
Role of ponticulin in pseudopod dynamics, cell-cell adhesion, and mechanical stability of an amoeboid membrane skeleton.桥粒斑蛋白在伪足动力学、细胞间黏附及变形虫样膜骨架机械稳定性中的作用
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Re-expression of ABP-120 rescues cytoskeletal, motility, and phagocytosis defects of ABP-120- Dictyostelium mutants.ABP - 120的重新表达挽救了ABP - 120缺失的盘基网柄菌突变体的细胞骨架、运动性和吞噬作用缺陷。
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Three-dimensional dynamics of pseudopod formation and the regulation of turning during the motility cycle of Dictyostelium.盘基网柄菌运动周期中伪足形成的三维动力学及转向调控
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7
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Ponticulin, a developmentally-regulated plasma membrane glycoprotein, mediates actin binding and nucleation.桥粒芯蛋白,一种受发育调控的质膜糖蛋白,介导肌动蛋白结合和成核。
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Indirect immunofluorescence localization of ponticulin in motile cells.桥粒芯蛋白在运动细胞中的间接免疫荧光定位。
Cell Motil Cytoskeleton. 1989;13(4):245-63. doi: 10.1002/cm.970130404.
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Targeted disruption of the ABP-120 gene leads to cells with altered motility.ABP - 120基因的靶向破坏导致细胞运动性改变。
J Cell Biol. 1992 Feb;116(4):943-55. doi: 10.1083/jcb.116.4.943.

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Supervillin (p205): A novel membrane-associated, F-actin-binding protein in the villin/gelsolin superfamily.supervillin(p205):一种在绒毛蛋白/凝溶胶蛋白超家族中新型的膜相关F-肌动蛋白结合蛋白。
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8
ICAMs redistributed by chemokines to cellular uropods as a mechanism for recruitment of T lymphocytes.细胞间黏附分子(ICAMs)通过趋化因子重新分布至细胞尾足,作为募集T淋巴细胞的一种机制。
J Cell Biol. 1997 Apr 21;137(2):493-508. doi: 10.1083/jcb.137.2.493.
9
Re-expression of ABP-120 rescues cytoskeletal, motility, and phagocytosis defects of ABP-120- Dictyostelium mutants.ABP - 120的重新表达挽救了ABP - 120缺失的盘基网柄菌突变体的细胞骨架、运动性和吞噬作用缺陷。
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本文引用的文献

1
The unconventional myosin encoded by the myoA gene plays a role in Dictyostelium motility.由肌动蛋白A基因编码的非常规肌球蛋白在盘基网柄菌的运动中发挥作用。
Mol Biol Cell. 1993 Feb;4(2):233-46. doi: 10.1091/mbc.4.2.233.
2
HIV-induced syncytia of a T cell line form single giant pseudopods and are motile.HIV诱导的T细胞系多核巨细胞形成单个巨大伪足且具有运动性。
J Cell Sci. 1993 Nov;106 ( Pt 3):941-53. doi: 10.1242/jcs.106.3.941.
3
Life at the leading edge: the formation of cell protrusions.前沿的生命:细胞突起的形成。
Annu Rev Cell Biol. 1993;9:411-44. doi: 10.1146/annurev.cb.09.110193.002211.
4
Three-dimensional dynamics of pseudopod formation and the regulation of turning during the motility cycle of Dictyostelium.盘基网柄菌运动周期中伪足形成的三维动力学及转向调控
Cell Motil Cytoskeleton. 1994;27(1):1-12. doi: 10.1002/cm.970270102.
5
Mechanisms of leukocyte motility and chemotaxis.白细胞运动和趋化性的机制。
Curr Opin Immunol. 1994 Feb;6(1):113-24. doi: 10.1016/0952-7915(94)90042-6.
6
Ponticulin is the major high affinity link between the plasma membrane and the cortical actin network in Dictyostelium.桥粒斑蛋白是盘基网柄菌质膜与皮质肌动蛋白网络之间主要的高亲和力连接物。
J Cell Biol. 1994 Sep;126(6):1433-44. doi: 10.1083/jcb.126.6.1433.
7
Ponticulin is an atypical membrane protein.桥粒芯蛋白是一种非典型膜蛋白。
J Cell Biol. 1994 Sep;126(6):1421-31. doi: 10.1083/jcb.126.6.1421.
8
3D analysis of cell movement during normal and myosin-II-null cell morphogenesis in dictyostelium.盘基网柄菌正常及肌球蛋白-II缺失细胞形态发生过程中细胞运动的三维分析
Dev Biol. 1995 Jan;167(1):118-29. doi: 10.1006/dbio.1995.1011.
9
Cellular plasma membrane domains.细胞质膜结构域
Mol Membr Biol. 1995 Jan-Mar;12(1):89-91. doi: 10.3109/09687689509038501.
10
Cell-substrate interactions and locomotion of Dictyostelium wild-type and mutants defective in three cytoskeletal proteins: a study using quantitative reflection interference contrast microscopy.盘基网柄菌野生型及三种细胞骨架蛋白缺陷型突变体的细胞-底物相互作用与运动:一项使用定量反射干涉对比显微镜的研究
Biophys J. 1995 Mar;68(3):1177-90. doi: 10.1016/S0006-3495(95)80294-8.

桥粒芯蛋白在伪足的位置稳定中发挥作用。

Ponticulin plays a role in the positional stabilization of pseudopods.

作者信息

Shutt D C, Wessels D, Wagenknecht K, Chandrasekhar A, Hitt A L, Luna E J, Soll D R

机构信息

Department of Biological Sciences, University of Iowa, Iowa City 52242, USA.

出版信息

J Cell Biol. 1995 Dec;131(6 Pt 1):1495-506. doi: 10.1083/jcb.131.6.1495.

DOI:10.1083/jcb.131.6.1495
PMID:8522606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2120683/
Abstract

Ponticulin is a 17-kD glycoprotein that represents a major high affinity link between the plasma membrane and the cortical actin network of Dictyostelium. To assess the role of ponticulin in pseudopod extension and retraction, the motile behavior of two independently generated mutants lacking ponticulin was analyzed using computer-assisted two- and three-dimensional motion analysis systems. More than half of the lateral pseudopods formed off the substratum by ponticulin-minus cells slipped relative to the substratum during extension and retraction. In contrast, all pseudopods formed off the substratum by wild-type cells were positionally fixed in relation to the substratum. Ponticulin-minus cells also formed a greater proportion of both anterior and lateral pseudopods off the substratum and absorbed a greater proportion of lateral pseudopods into the uropod than wild-type cells. In a spatial gradient of cAMP, ponticulin-minus cells were less efficient in tracking the source of chemoattractant. Since ponticulin-minus cells extend and retract pseudopods with the same time course as wild-type cells, these behavioral defects in ponticulin-minus cells appear to be the consequence of pseudopod slippage. These results demonstrate that pseudopods formed off the substratum by wild-type cells are positionally fixed in relation to the substratum, that ponticulin is required for positional stabilization, and that the loss of ponticulin and the concomitant loss of positional stability of pseudopods correlate with a decrease in the efficiency of chemotaxis.

摘要

桥粒芯蛋白是一种17-kD糖蛋白,是盘基网柄菌质膜与皮质肌动蛋白网络之间的主要高亲和力连接物。为了评估桥粒芯蛋白在伪足伸展和收缩中的作用,使用计算机辅助的二维和三维运动分析系统分析了两个独立产生的缺乏桥粒芯蛋白的突变体的运动行为。在伸展和收缩过程中,超过一半由缺失桥粒芯蛋白的细胞在基质外形成的侧向伪足相对于基质滑动。相比之下,野生型细胞在基质外形成的所有伪足相对于基质的位置都是固定的。与野生型细胞相比,缺失桥粒芯蛋白的细胞在基质外形成的前侧和侧向伪足的比例也更高,并且更多的侧向伪足被吸收到尾足中。在cAMP的空间梯度中,缺失桥粒芯蛋白的细胞追踪趋化因子来源的效率较低。由于缺失桥粒芯蛋白的细胞与野生型细胞在相同的时间进程内伸展和收缩伪足,这些缺失桥粒芯蛋白的细胞的行为缺陷似乎是伪足滑动的结果。这些结果表明,野生型细胞在基质外形成的伪足相对于基质的位置是固定的,桥粒芯蛋白是位置稳定所必需的,并且桥粒芯蛋白的缺失以及伪足位置稳定性的随之丧失与趋化性效率的降低相关。