Data · dataset · 2020
Supplementary material - Impact of Na+ permeation on collective migration of pulmonary arterial endothelial cells (Xu et al)
Listed in DataCite
Endothelial migration is necessary for wound healing and angiogenesis.
Description
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.
Links
Where it is published
- Repository landing page figshare.com/articles/dataset/Supplementary_material_-_Impact_of_Na_permeat… ↗
landing page · from DataCite
- Repository landing page figshare.com/articles/dataset/Supplementary_material_-_Impact_of_Na_permeat… ↗
landing page · from DataCite
- DOI doi.org/10.6084/m9.figshare.12909863 ↗
DOI / persistent id · from DataCite
- DOI doi.org/10.6084/m9.figshare.12909863.v1 ↗
DOI / persistent id · from DataCite
Documentation and papers
Catalogue records · 4
- DataCite API api.datacite.org/dois/10.6084/m9.figshare.12909863.v1 ↗
metadata API · from DataCite
- DataCite API api.datacite.org/dois/10.6084/m9.figshare.12909863 ↗
metadata API · from DataCite
- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.12909863.v1 ↗
catalogue entry · from DataCite
- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.12909863 ↗
catalogue entry · from DataCite
Topics
- Stated by source
- Basic medicine · Basic medicine
Provenance · 2 source records, 10 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| DataCite | 10.6084/m9.figshare.12909863 | 11 d ago | JSON v1 |
| DataCite | 10.6084/m9.figshare.12909863.v1 | 11 d ago | JSON v1 |
| Field | Assertion | Extractor | Evidence |
|---|---|---|---|
| access_level | source · DataCite | connector:datacite@1.0.0 | /data/attributes/rightsList |
| byte_size | source · DataCite | connector:datacite@1.0.0 | |
| concepts[field].fos:basic-medicine | source · DataCite | connector:datacite@1.0.0 | |
| concepts[field].fos:basic-medicine | source · DataCite | connector:datacite@1.0.0 | |
| created_date | source · DataCite | connector:datacite@1.0.0 | |
| description | source · DataCite | connector:datacite@1.0.0 | /data/attributes/descriptions |
| license | source · DataCite | connector:datacite@1.0.0 | /data/attributes/rightsList |
| publication_date | source · DataCite | connector:datacite@1.0.0 | /data/attributes/dates |
| title | source · DataCite | connector:datacite@1.0.0 | /data/attributes/titles/0/title |
| updated_date | source · DataCite | connector:datacite@1.0.0 |