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A polarized Ca2+, diacylglycerol and STIM1 signalling system regulates directed cell migration.


ABSTRACT: Ca(2+) signals control cell migration by regulating forward movement and cell adhesion. However, it is not well understood how Ca(2+)-regulatory proteins and second messengers are spatially organized in migrating cells. Here we show that receptor tyrosine kinase and phospholipase C signalling are restricted to the front of migrating endothelial leader cells, triggering local Ca(2+) pulses, local depletion of Ca(2+) in the endoplasmic reticulum and local activation of STIM1, supporting pulsatile front retraction and adhesion. At the same time, the mediator of store-operated Ca(2+) influx, STIM1, is transported by microtubule plus ends to the front. Furthermore, higher Ca(2+) pump rates in the front relative to the back of the plasma membrane enable effective local Ca(2+) signalling by locally decreasing basal Ca(2+). Finally, polarized phospholipase C signalling generates a diacylglycerol gradient towards the front that promotes persistent forward migration. Thus, cells employ an integrated Ca(2+) control system with polarized Ca(2+) signalling proteins and second messengers to synergistically promote directed cell migration.

SUBMITTER: Tsai FC 

PROVIDER: S-EPMC3953390 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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A polarized Ca2+, diacylglycerol and STIM1 signalling system regulates directed cell migration.

Tsai Feng-Chiao FC   Seki Akiko A   Yang Hee Won HW   Hayer Arnold A   Carrasco Silvia S   Malmersjö Seth S   Meyer Tobias T  

Nature cell biology 20140126 2


Ca(2+) signals control cell migration by regulating forward movement and cell adhesion. However, it is not well understood how Ca(2+)-regulatory proteins and second messengers are spatially organized in migrating cells. Here we show that receptor tyrosine kinase and phospholipase C signalling are restricted to the front of migrating endothelial leader cells, triggering local Ca(2+) pulses, local depletion of Ca(2+) in the endoplasmic reticulum and local activation of STIM1, supporting pulsatile  ...[more]

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