Skewing of the population balance of lymphoid and myeloid cells by secreted and intracellular osteopontin.

dc.contributor.author

Kanayama, Masashi

dc.contributor.author

Xu, Shengjie

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Danzaki, Keiko

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Gibson, Jason R

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Inoue, Makoto

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Gregory, Simon G

dc.contributor.author

Shinohara, Mari L

dc.date.accessioned

2018-11-11T21:11:03Z

dc.date.available

2018-11-11T21:11:03Z

dc.date.issued

2017-09

dc.date.updated

2018-11-11T21:10:57Z

dc.description.abstract

The balance of myeloid populations and lymphoid populations must be well controlled. Here we found that osteopontin (OPN) skewed this balance during pathogenic conditions such as infection and autoimmunity. Notably, two isoforms of OPN exerted distinct effects in shifting this balance through cell-type-specific regulation of apoptosis. Intracellular OPN (iOPN) diminished the population size of myeloid progenitor cells and myeloid cells, and secreted OPN (sOPN) increase the population size of lymphoid cells. The total effect of OPN on skewing the leukocyte population balance was observed as host sensitivity to early systemic infection with Candida albicans and T cell-mediated colitis. Our study suggests previously unknown detrimental roles for two OPN isoforms in causing the imbalance of leukocyte populations.

dc.identifier

ni.3791

dc.identifier.issn

1529-2908

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1529-2916

dc.identifier.uri

https://hdl.handle.net/10161/17648

dc.language

eng

dc.publisher

Springer Science and Business Media LLC

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Nature immunology

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10.1038/ni.3791

dc.subject

Lymphocytes

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T-Lymphocytes

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Myeloid Cells

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Animals

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Mice, Knockout

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Mice

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Candida albicans

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Infection

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Candidiasis

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Colitis

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Autoimmune Diseases

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Protein Isoforms

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Enzyme-Linked Immunosorbent Assay

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Flow Cytometry

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Reverse Transcriptase Polymerase Chain Reaction

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Apoptosis

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Lymphopoiesis

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Myelopoiesis

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Cell Proliferation

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Osteopontin

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Real-Time Polymerase Chain Reaction

dc.title

Skewing of the population balance of lymphoid and myeloid cells by secreted and intracellular osteopontin.

dc.type

Journal article

duke.contributor.orcid

Gregory, Simon G|0000-0002-7805-1743

duke.contributor.orcid

Shinohara, Mari L|0000-0002-6808-9844

pubs.begin-page

973

pubs.end-page

984

pubs.issue

9

pubs.organisational-group

School of Medicine

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Duke

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Duke Cancer Institute

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Institutes and Centers

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Duke Molecular Physiology Institute

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Molecular Genetics and Microbiology

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Basic Science Departments

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Neurology, MS & Neuroimmunology

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Neurology

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Clinical Science Departments

pubs.organisational-group

Immunology

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Student

pubs.publication-status

Published

pubs.volume

18

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