DefinitionThis section has been translated automatically.
T-plastin is an actin-binding protein that plays an important role in the stabilization of the cytoskeleton. It belongs to the plastin family. Plastins are a family of actin-binding proteins.
T-plastin is expressed differently in normal and malignant cells. Through its cross-linking with actin filaments, T-plastin is involved in cell motility and contributes to the formation and stabilization of the actin network.
General informationThis section has been translated automatically.
Function of T-Plastin:
- Supports cell migration, cell adhesion and cell mechanics.
- Plays a role in the immune response by influencing the dynamics of the actin cytoskeleton in immune cells.
- Involvement in tumor biology: T-plastin is associated with increased cell invasiveness in some tumor entities.
- In neuronal tissue relevant for the plasticity and function of nerve cells.
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Clinical pictureThis section has been translated automatically.
Tissue specificity: T-plastin is mainly expressed in T lymphocytes and other non-hematopoietic cells.
Tumor marker: Overexpression of PLS3 may correlate with tumor progression and metastasis in certain tumor entities.
Spinal muscular atrophy (SMA): PLS3 has been identified as a potential modifier of the disease - high PLS3 expression may positively influence disease progression.
Autoimmune diseases: Dysregulation of T-plastin expression may be associated with immunologic dysfunction.
Note(s)This section has been translated automatically.
T-plastin is considered to be a key player in the mechanisms of calcineurin/NFAT-dependent keratinocyte migration. This may explain the wound healing defects observed in patients undergoing long-term treatment with a calcineurin inhibitor (Brun C et al. 2014)
LiteratureThis section has been translated automatically.
- Brun C et al. (2014) T-plastin expression downstream to the calcineurin/NFAT pathway is involved in keratinocyte migration. PLoS One. 2014 Sep 16;9(9):e104700.
- Garbett D et al. (2020) T-Plastin reinforces membrane protrusions to bridge matrix gaps during cell migration. Nat Commun 11:4818.