PXD015810 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Pacific oyster phagosome LC-MSMS |
Description | Phagosomes are task-force organelles of innate immune systems responsible for the recognition, processing, and ultimately destruction of invading microorganisms. Among invertebrate and vertebrate species, evolutionary diversity and continuity abound in the protein machinery executing this coordinately regulated process, though its dynamics and full scope of regulators remain incompletely understood. In order to clarify molecular mechanisms underlying phagocytosis, we studied phagocyte response to beads and Vibrio species, using hemocytes of the Pacific oysters (Crassostrea gigas) as a marine invertebrate model. Phagosomes from different stages of phagocytosis were isolated by density-gradient centrifugation, and more than 400 phagosome-associated proteins were subsequently identified via high-throughput quantitative proteomics. In modeling key networks of phagosomal protein-protein interactions, our results support the essential roles of several processes driving phagosome formation and maturation, including actin cytoskeleton remodeling, and signal transduction by myosin and Rab proteins. In further quantitative proteomic analysis, trends of both upregulation and downregulation of protein expression were observed proteins during phagosome formation and maturation. Notably, the signal transducers CgRhoGDI and CgPI4K were implicated. In addition, six Rab proteins including Rab1, Rab2, Rab7, Rab11, RaB21, and Rab33 were also identified as active regulators or mediators in hemocyte phagocytosis. Our current work illustrates the diversity and dynamic interplay of phagosomal proteins, providing a framework for better understanding host-microbe interactions during phagosome formation and maturation in under-examined invertebrate species. |
HostingRepository | PRIDE |
AnnounceDate | 2020-04-27 |
AnnouncementXML | Submission_2020-04-26_23:18:13.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Huawei MU |
SpeciesList | scientific name: Crassostrea gigas; NCBI TaxID: 29159; |
ModificationList | monohydroxylated residue; deamidated residue |
Instrument | LTQ Orbitrap Elite |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2019-10-14 02:05:11 | ID requested | |
⏵ 1 | 2020-04-26 23:18:14 | announced | |
2 | 2024-10-22 05:02:39 | announced | 2024-10-22: Updated project metadata. |
Publication List
Mao F, Mu H, Wong NK, Liu K, Song J, Qiu J, Lin Y, Zhang X, Xu D, Xiang Z, Li J, Zhang Y, Yu Z, Hemocyte phagosomal proteome is dynamically shaped by cytoskeleton remodeling and interorganellar communication with endoplasmic reticulum during phagocytosis in a marine invertebrate, Crassostrea gigas. Sci Rep, 10(1):6577(2020) [pubmed] |
Keyword List
submitter keyword: phagosome, oyster, actin remodeling, innate immunity |
Contact List
Ziniu Yu |
contact affiliation | Institute of Oceanology, Chinese Academy of Sciences, 164 West Xingang Road, Guangzhou 510301, China. |
contact email | carlzyu@scsio.ac.cn |
lab head | |
Huawei MU |
contact affiliation | USTC |
contact email | huaweimu@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD015810
- Label: PRIDE project
- Name: Pacific oyster phagosome LC-MSMS