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Leader cell PLCγ1 activation during keratinocyte collective migration is induced by EGFR localization and clustering.


ABSTRACT: Re-epithelialization is a critical step in wound healing and results from the collective migration of keratinocytes. Previous work demonstrated that immobilized, but not soluble, epidermal growth factor (EGF) resulted in leader cell-specific activation of phospholipase C gamma 1 (PLCγ1) in HaCaT keratinocytes, and that this PLCγ1 activation was necessary to drive persistent cell migration. To determine the mechanism responsible for wound edge-localized PLCγ1 activation, we examined differences in cell area, cell-cell interactions, and EGF receptor (EGFR) localization between wound edge and bulk cells treated with vehicle, soluble EGF, or immobilized EGF. Our results support a multistep mechanism where EGFR translocation from the lateral membrane to the basolateral/basal membrane allows clustering in response to immobilized EGF. This analysis of factors regulating PLCγ1 activation is a crucial step toward developing therapies or wound dressings capable of modulating this signal and, consequently, cell migration.

SUBMITTER: Kim CS 

PROVIDER: S-EPMC6764804 | biostudies-other | 2019 Sep

REPOSITORIES: biostudies-other

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Leader cell PLCγ1 activation during keratinocyte collective migration is induced by EGFR localization and clustering.

Kim Chloe S CS   Yang Xinhai X   Jacobsen Sarah S   Masters Kristyn S KS   Kreeger Pamela K PK  

Bioengineering & translational medicine 20190626 3


Re-epithelialization is a critical step in wound healing and results from the collective migration of keratinocytes. Previous work demonstrated that immobilized, but not soluble, epidermal growth factor (EGF) resulted in leader cell-specific activation of phospholipase C gamma 1 (PLCγ1) in HaCaT keratinocytes, and that this PLCγ1 activation was necessary to drive persistent cell migration. To determine the mechanism responsible for wound edge-localized PLCγ1 activation, we examined differences i  ...[more]

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