Label-Free Quantitative Proteomics to Explore the Action Mechanism of the Pharmaceutical-Grade Triticum vulgare Extract in Speeding Up Keratinocyte Healing.
Elva MorrettaAntonella D'AgostinoElisabetta CasseseBarbara MaglioneAntonello PetrellaChiara SchiraldiMaria Chiara MontiPublished in: Molecules (Basel, Switzerland) (2022)
Plant extracts have shown beneficial properties in terms of skin repair, promoting wound healing through a plethora of mechanisms. In particular, the poly-/oligosaccharidic aqueous extract of Triticum vulgare (TVE), as well as TVE-based products, shows interesting biological assets, hastening wound repair. Indeed, TVE acts in the treatment of tissue regeneration mainly on decubitus and venous leg ulcers. Moreover, on scratched monolayers, TVE prompts HaCat cell migration, correctly modulating the expression of metalloproteases toward a physiological matrix remodeling. Here, using the same HaCat-based in vitro scratch model, the TVE effect has been investigated thanks to an LFQ proteomic analysis of HaCat secretomes and immunoblotting. Indeed, the unbiased TVE effect on secreted proteins has not yet been fully understood, and it could be helpful to obtain a comprehensive picture of its bio-pharmacological profile. It has emerged that TVE treatment induces significant up-regulation of several proteins in the secretome (153 to be exact) whereas only a few were down-regulated (72 to be exact). Interestingly, many of the up-regulated proteins are implicated in promoting wound-healing-related processes, such as modulating cell-cell interaction and communication, cell proliferation and differentiation, and prompting cell adhesion and migration.
Keyphrases
- wound healing
- label free
- cell migration
- cell proliferation
- cell adhesion
- single cell
- oxidative stress
- stem cells
- poor prognosis
- signaling pathway
- transcription factor
- cell therapy
- density functional theory
- mass spectrometry
- cell cycle
- combination therapy
- essential oil
- bone marrow
- replacement therapy
- smoking cessation
- atomic force microscopy