Optogenetic toolkit reveals the role of Ca2+ sparklets in coordinated cell migration.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 27190091.
- Also identified by DOI 10.1073/pnas.1518412113 and PMC identifier 4889354.
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Abstract
Cell migration is controlled by various Ca(2+) signals. Local Ca(2+) signals, in particular, have been identified as versatile modulators of cell migration because of their spatiotemporal diversity. However, little is known about how local Ca(2+) signals coordinate between the front and rear regions in directionally migrating cells. Here, we elucidate the spatial role of local Ca(2+) signals in directed cell migration through combinatorial application of an optogenetic toolkit. An optically guided cell migration approach revealed the existence of Ca(2+) sparklets mediated by L-type voltage-dependent Ca(2+) channels in the rear part of migrating cells. Notably, we found that this locally concentrated Ca(2+) influx acts as an essential transducer in establishing a global front-to-rear increasing Ca(2+) gradient. This asymmetrical Ca(2+) gradient is crucial for maintaining front-rear morphological polarity by restricting spontaneous lamellipodia formation in the rear part of migrating cells. Collectively, our findings demonstrate a clear link between local Ca(2+) sparklets and front-rear coordination during directed cell migration.
Medical subject headings
- Calcium
- Calcium Channels, L-Type
- Calcium Signaling
- Cell Movement
- Human Umbilical Vein Endothelial Cells
- Optogenetics