In C2C12 myoblastic cells, thymosin beta‑4 and its sulphoxized form significantly accelerated wound closure.
In plain wordsIn mouse muscle cells in a dish, thymosin beta‑4 and its oxidised form sped up wound closure.
- Peptide
- Thymosin beta-4 (human)
- Outcome
- IncreaseWound closure of C2C12 myoblastic cells
- Study
mousen: not reported in source
C2C12 myoblastic cells- Outcome group
- Wound healing · Musculoskeletal
- Studied dose
- Dose not stated
Source sentences
We found that both Tβ4 and its sulphoxized form significantly accelerated wound closure and increased the chemotaxis of C2C12 myoblastic cells.