PXD056025 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Microvesicles Derived from Human Bronchial Epithelial Cells Regulate Macrophage Activation During Mycobacterium abscessus Infection |
| Description | Intercellular communication is important for host immunity in response to bacterial infections. Nontuberculous mycobacterium (NTM), such as Mycobacterium abscessus (M.ab), is a group of environmental bacteria that can cause severe lung infections in individuals with pre-existing lung conditions, including cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). There is limited knowledge understanding the interaction between airway epithelial cells and immune cells during NTM infections. In this study, we characterized microvesicles (MVs) released from M.ab-infected human bronchial epithelial cells and investigated the effect of these MVs on the activation and polarization of THP-1-derived macrophages in cell culture. Our results indicate that MVs released by M.ab-infected human bronchial epithelial cells stimulated the activation of M2-polarized macrophages in cell culture. Additionally, the proteomic analysis for isolated MVs showed that the proteins involved in the cell adhesion pathway were enriched in MVs from M.ab-infected human bronchial epithelial cells compared to the uninfected cells. Among those, the cell surface protein, intercellular adhesion molecule 1 (ICAM-1), regulated the MV internalization by recipient macrophages. In conclusion, our data suggests that in response to M.ab infection, human airway epithelial cells release MVs to modulate the activation of macrophages, which are key cells for mycobacterial intracellular survival in the host. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-03-30 |
| AnnouncementXML | Submission_2026-03-29_16:43:06.311.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Steven Hartson |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; scientific name: Mycobacterium abscessus (strain ATCC 19977 / DSM 44196 / CIP 104536 / JCM 13569 / NCTC 13031 / TMC 1543); NCBI TaxID: NEWT:561007; |
| ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Fusion |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-09-19 09:17:23 | ID requested | |
| ⏵ 1 | 2026-03-29 16:43:07 | announced | |
Publication List
| Guthrie CM, Meeker AC, Self AE, Ramos-Leyva A, Clark OL, Kotey SK, Hartson SD, Liang Y, Liu L, Tan X, Cheng Y, Infection. J Proteome Res, 24(5):2291-2301(2025) [pubmed] |
| 10.1021/acs.jproteome.4c00827; |
Keyword List
| submitter keyword: Extracellular Vesicles |
| Microvesicles |
| Epithelial Cells |
| Macrophages |
| Mycobacterium abscessus |
| Proteomics |
| Intracellular Communication |
Contact List
| Yong Cheng |
| contact affiliation | Department of Biochemistry and Molecular Biology, Oklahoma Center for Respiratory and Infectious Diseases, Oklahoma State University, Stillwater, Oklahoma, USA |
| contact email | ycheng@okstate.edu |
| lab head | |
| Steven Hartson |
| contact affiliation | Oklahoma State University |
| contact email | hartson.steve@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD056025
- Label: PRIDE project
- Name: Microvesicles Derived from Human Bronchial Epithelial Cells Regulate Macrophage Activation During Mycobacterium abscessus Infection