| Literature DB >> 27173494 |
Samantha J King1, Sreeja B Asokan1, Elizabeth M Haynes1, Seth P Zimmerman2, Jeremy D Rotty1, James G Alb1, Alicia Tagliatela1, Devon R Blake3, Irina P Lebedeva4, Daniel Marston5, Heath E Johnson6, Maddy Parsons7, Norman E Sharpless8, Brian Kuhlman2, Jason M Haugh6, James E Bear9.
Abstract
Haptotaxis is the process by which cells respond to gradients of substrate-bound cues, such as extracellular matrix proteins (ECM); however, the cellular mechanism of this response remains poorly understood and has mainly been studied by comparing cell behavior on uniform ECMs with different concentrations of components. To study haptotaxis in response to gradients, we utilized microfluidic chambers to generate gradients of the ECM protein fibronectin, and imaged the cell migration response. Lamellipodia are fan-shaped protrusions that are common in migrating cells. Here, we define a new function for lamellipodia and the cellular mechanism required for haptotaxis - differential actin and lamellipodial protrusion dynamics lead to biased cell migration. Modest differences in lamellipodial dynamics occurring over time periods of seconds to minutes are summed over hours to produce differential whole cell movement towards higher concentrations of fibronectin. We identify a specific subset of lamellipodia regulators as being crucial for haptotaxis. Numerous studies have linked components of this pathway to cancer metastasis and, consistent with this, we find that expression of the oncogenic Rac1 P29S mutation abrogates haptotaxis. Finally, we show that haptotaxis also operates through this pathway in 3D environments.Entities:
Keywords: Arp2/3; Directed migration; Haptotaxis; Lamellipodia
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Year: 2016 PMID: 27173494 PMCID: PMC4920251 DOI: 10.1242/jcs.184507
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285