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Data · dataset · 2020

Supplementary material - Impact of Na+ permeation on collective migration of pulmonary arterial endothelial cells (Xu et al)

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Endothelial migration is necessary for wound healing and angiogenesis.

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Na + has been incriminated as an important cellular signal mediating migration, although the ion channels regulating Na + permeation that contribute to migration remain poorly understood. First, we studied the contribution of extracellular Na + to scratch wound healing.

Second, we studied the effects of Na + channel inhibitors inhibiting ENaC, NCX, Orai1, and/or TRPC4 to scratch wound healing. Third, we studied the contribution of Orai1 expression to scratch and non-scratch wound healing in the presence and absence of extracellular Na + . All studies were conducted using pulmonary artery endothelial cells (PAEC).

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We found that permeation of extracellular Na + is necessary for efficient and cohesive migration of PAEC monolayers. The processes of wound healing displayed two phases: a fast healing phase within 5 hours followed by a slow-healing phase between 5 and 24 hours. Among the examined Na + channels, Na + permeation through ENaC produced prompt and largest effect on wound healing, Na + permeation through NCX produced small and delayed effect, Na + permeation through Orai1 produced small and short-term effect, and Na + permeation through TRPC1/4 produced insignificant effect.

Both extracellular Na + and Orai1 contribute to scratch wound healing, whereas only extracellular Na + but not Orai1 contributes to cell migration in the absence of injury.

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Basic medicine · Basic medicine
Provenance · 2 source records, 10 field assertions
SourceKeyLast seenRaw
DataCite10.6084/m9.figshare.1290986311 d agoJSON v1
DataCite10.6084/m9.figshare.12909863.v111 d agoJSON v1
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