Treponema pallidum enhances human monocyte migration and invasion by dysregulating the MMP/TIMP balance.
Cell Movement
Humans
Matrix Metalloproteinase 1
/ genetics
Matrix Metalloproteinase 9
/ genetics
Mitogen-Activated Protein Kinase 1
/ metabolism
Monocytes
/ physiology
NF-kappa B
/ metabolism
Signal Transduction
THP-1 Cells
Tissue Inhibitor of Metalloproteinase-1
/ genetics
Tissue Inhibitor of Metalloproteinase-2
/ genetics
Treponema pallidum
Invasion
MMP/TIMP imbalance
Migration
Monocyte
Treponema pallidum
Journal
International immunopharmacology
ISSN: 1878-1705
Titre abrégé: Int Immunopharmacol
Pays: Netherlands
ID NLM: 100965259
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
19
05
2019
revised:
24
06
2019
accepted:
05
07
2019
pubmed:
19
7
2019
medline:
7
3
2020
entrez:
19
7
2019
Statut:
ppublish
Résumé
Although the infiltration of monocytes into local lesions is an obvious pathological manifestation in the pathogenesis of syphilis, little is known about the role of metalloproteinase (MMP)/tissue inhibitor of metalloproteinases (TIMP) imbalance in the migration/invasion of THP-1 cells induced by Treponema pallidum (T. pallidum). The influence of T. pallidum on the invasion and migration of THP-1 cells was evaluated. Changes in the MMP/TIMP balance and the mechanisms underlying the involvement of the MAPK and NF-κB signaling pathways in this process were explored. T. pallidum induced the migration/invasion of THP-1 cells and the mRNA and protein expression of MMP-1, MMP-9 and TIMP-1. The mRNA expression of TIMP-2 was reduced, and the protein expression of TIMP-2 was not changed. The MMP-1/TIMP-1, MMP-1/TIMP-2, MMP-9/TIMP-1 and MMP-9/TIMP-2 ratios were increased. Inhibition of JNK, MEK/ERK, p38 MAPK and NF-κB significantly decreased the MMP/TIMP ratio and ultimately suppressed the migration/invasion of THP-1 cells. These findings revealed that MMP/TIMP imbalances induced by T. pallidum enhanced THP-1 cell migration and invasion via MAPK and NF-κB signaling pathway activation, which revealed a novel step in syphilis pathophysiology.
Identifiants
pubmed: 31319358
pii: S1567-5769(19)31064-1
doi: 10.1016/j.intimp.2019.105744
pii:
doi:
Substances chimiques
NF-kappa B
0
TIMP1 protein, human
0
TIMP2 protein, human
0
Tissue Inhibitor of Metalloproteinase-1
0
Tissue Inhibitor of Metalloproteinase-2
127497-59-0
Mitogen-Activated Protein Kinase 1
EC 2.7.11.24
MMP9 protein, human
EC 3.4.24.35
Matrix Metalloproteinase 9
EC 3.4.24.35
MMP1 protein, human
EC 3.4.24.7
Matrix Metalloproteinase 1
EC 3.4.24.7
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105744Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.