Tofacitinib Regulates Endostatin via Effects on CD147 and Cathepsin S.
Humans
Basigin
/ metabolism
Piperidines
/ pharmacology
Endostatins
/ metabolism
Pyrimidines
/ pharmacology
Cathepsins
/ metabolism
Arthritis, Rheumatoid
/ drug therapy
Matrix Metalloproteinase 9
/ metabolism
STAT3 Transcription Factor
/ metabolism
Neovascularization, Pathologic
/ metabolism
Angiogenesis Inhibitors
/ pharmacology
Female
Middle Aged
Male
Pyrroles
/ pharmacology
Cell Line
CD147/EMMPRIN
STAT3
angiogenesis
endostatin
miR-146a-5p 1
rheumatoid arthritis (RA)
tofacitinib
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
02 Jul 2024
02 Jul 2024
Historique:
received:
03
06
2024
revised:
23
06
2024
accepted:
25
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
Angiogenesis is critical for rheumatoid arthritis (RA) progression. The effects of tofacitinib, a JAK-STAT inhibitor used for RA treatment, on angiogenesis in RA are unclear. We, therefore, evaluated the levels of angiogenic factors in two systems of a human co-culture of fibroblast (HT1080) and monocytic (U937) cell lines treated with tofacitinib and in serum samples from RA patients before and after six months of tofacitinib treatment. Tofacitinib reduced CD147 levels, matrix metalloproteinase-9 (MMP-9) activity, and angiogenic potential but increased endostatin levels and secreted proteasome 20S activity. In vitro, tofacitinib did not change CD147 mRNA but increased miR-146a-5p expression and reduced STAT3 phosphorylation. We recently showed that CD147 regulates the ability of MMP-9 and secreted proteasome 20S to cleave collagen XVIIIA into endostatin. We show here that tofacitinib-enhanced endostatin levels are mediated by CD147, as CD147-siRNA or an anti-CD147 antibody blocked proteasome 20S activity. The correlation between CD147 and different disease severity scores supported this role. Lastly, tofacitinib reduced endostatin' s degradation by inhibiting cathepsin S activity and recombinant cathepsin S reversed this in both systems. Thus, tofacitinib inhibits angiogenesis by reducing pro-angiogenic factors and enhancing the anti-angiogenic factor endostatin in a dual effect mediated partly through CD147 and partly through cathepsin S.
Identifiants
pubmed: 39000375
pii: ijms25137267
doi: 10.3390/ijms25137267
pii:
doi:
Substances chimiques
Basigin
136894-56-9
tofacitinib
87LA6FU830
Piperidines
0
Endostatins
0
Pyrimidines
0
cathepsin S
EC 3.4.22.27
Cathepsins
EC 3.4.-
BSG protein, human
0
Matrix Metalloproteinase 9
EC 3.4.24.35
STAT3 Transcription Factor
0
Angiogenesis Inhibitors
0
Pyrroles
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Pfizer Pharmaceuticals, Israel LTD
ID : WI219474