Macrophages Inability to Mediate Adherent-Invasive Replication is Linked to Autophagy in Crohn's Disease Patients.
Clicks: 334
ID: 79839
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
30.0
/100
334 views
42 readers
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #16 of 84 articles by views in Cells
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
The macrophages from Crohn's Disease (CD) patients are defective to control the replication of CD-associated adherent-invasive (AIEC). We aimed to identify the host factors associated with AIEC replication focusing on polymorphisms related to autophagy. Peripheral blood monocyte-derived macrophages (MDM), obtained from 95 CD patient, 30 ulcerative colitis (UC) patients and 15 healthy subjects, were genotyped for several CD-associated polymorphisms. AIEC bacteria survival increased within MDM from CD patients compared to UC ( = 0.0019). AIEC bacteria survival increased in patients with CD-associated polymorphism ( = 0.05) and reduced in those with CD-associated polymorphisms ( = 0.026) and ( = 0.033). AIEC infection led to an increase of pro-inflammatory cytokines IL-1β ( < 0.0001) and TNF-α ( < 0.0001) in CD macrophages. ULK-1 expression increased in AIEC-infected MDM from CD patients compared to MDM from UC patients or healthy subjects ( = 0.0056) and correlated with AIEC survival ( = 0.0013). Moreover, the expression of ULK-1 phosphorylation on Serine 757 decreased following to AIEC infection ( < 0.0001). Short-term silencing of ULK-1 and IRGM genes restricted and promote, respectively, AIEC survival within MDM ( = 0.0018 and = 0.0291). In conclusion, the macrophage defect to mediate AIEC clearance in CD patients is linked to polymorphisms related to autophagy such as IRGM and ULK-1.
| Reference Key |
buisson2019macrophagescells
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Buisson, Anthony;Douadi, Clara;Ouchchane, Lemlih;Goutte, Marion;Hugot, Jean-Pierre;Dubois, Anaëlle;Minet-Quinard, Régine;Bouvier, Damien;Bommelaer, Gilles;Vazeille, Emilie;Barnich, Nicolas; |
| Journal | Cells |
| Year | 2019 |
| DOI |
E1394
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.