Aging Overview

External factors

External factors: Chitosan
Aging type: Prevent
Aging characteristic:
Category: Chemical compounds
Phenotype: Aging
Experimental category: L
Tissue type: Foreskin
Cell name: Fibroblast
PMID: 29081244
Experiment: SA-β-gal activity assay
Description: SA-β-gal activity assay:cellCompared to fibroblasts always on TCPS without culturing on chitosan (w/o treatment), cells after chitosan treatment for 3 days significantly decreased the percentage of SA β-gal-positive cells from about 20% to less than 10% cultured on chitosan for 5 DIV increased the percentage of SA β-gal-positive cells.


Regulatory relationship

Regulatory pathway: TGF-β
R-EF-Pathway: Downregulation
Official symbol(s): TGFB1
Pathway experiment: SA-β-gal activity assay//Western blot
Pathway description: SA-β-gal activity assay:The tendency of cell senescence increased with increasing the TGF-b concentration. Therefore, we assumed chitosan could suppress TGF-β signaling to delay the progress of fibroblast senescence.Western blot:compared to cells cultured on TCPS, only cells treated by chitosan showed significantly lower expression of TGF-b, Smad2/3 and pSmad2/3 .


Aging network

Annotation:

The green line represents Upregulation.

The purple line represents Downregulation.

The orange line represents Activation.

The yellow line represents Inhibition.

The gray line represents Unclear.



Pathway view