Cell division orientation is coupled to cell-cell adhesion by the E-cadherin/LGN complex

被引:91
|
作者
Gloerich, Martijn [1 ,3 ]
Bianchini, Julie M. [1 ]
Siemers, Kathleen A. [1 ]
Cohen, Daniel J. [1 ]
Nelson, W. James [1 ,2 ]
机构
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[3] Univ Med Ctr Utrecht, Ctr Mol Med, Mol Canc Res, Univ Weg 100, NL-3584CG Utrecht, Netherlands
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
关键词
SPINDLE ORIENTATION; ADHERENS JUNCTIONS; ASYMMETRIC DIVISION; CATENIN; PROTEINS; POLARITY; NUMA; LGN; MOLECULES; DYNEIN;
D O I
10.1038/ncomms13996
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Both cell-cell adhesion and oriented cell division play prominent roles in establishing tissue architecture, but it is unclear how they might be coordinated. Here, we demonstrate that the cell-cell adhesion protein E-cadherin functions as an instructive cue for cell division orientation. This is mediated by the evolutionarily conserved LGN/NuMA complex, which regulates cortical attachments of astral spindle microtubules. We show that LGN, which adopts a three-dimensional structure similar to cadherin-bound catenins, binds directly to the E-cadherin cytosolic tail and thereby localizes at cell-cell adhesions. On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cadherin to locally form the LGN/NuMA complex. This mediates the stabilization of cortical associations of astral microtubules at cell-cell adhesions to orient the mitotic spindle. Our results show how E-cadherin instructs the assembly of the LGN/NuMA complex at cell-cell contacts, and define a mechanism that couples cell division orientation to intercellular adhesion.
引用
收藏
页数:11
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