Study type: In vivo/preclinical · Status: Verified against declared source
Thymosin β4 reverses phenotypic polarization of glial cells and cognitive impairment via negative regulation of NF-κB signaling axis in APP/PS1 mice.
Journal of neuroinflammation · 2021
Study scale: Following NORT, mice were assessed in the Y maze.
Abstract only: Open source record
Product or molecular entity relationships
- Thymosin Beta-4 (TB500): Exact entity relationship. Legacy citation custody associates this source with the catalog record; no product-relevance conclusion is implied.
Plain-language verified summary
Question
Thymosin β4 (Tβ4) is the most abundant member of the β-thymosins and plays an important role in the control of actin polymerization in eukaryotic cells.
Methods
The online version contains supplementary material available at 10.1186/s12974-021-02166-3.
Scale or participants
Following NORT, mice were assessed in the Y maze.
Key findings
Thymosin β4 (Tβ4) is the most abundant member of the β-thymosins and plays an important role in the control of actin polymerization in eukaryotic cells.
Limitations and uncertainty
This also applied to Sholl analysis quantification when we summarized the represented microglia profile.
Verified against declared source. Verification is limited to the declared source and review scope. It does not mean independent replication or establish efficacy, safety, or suitability.