Interleukin‐34, a comprehensive review. Issue 5 (1st August 2018)
- Record Type:
- Journal Article
- Title:
- Interleukin‐34, a comprehensive review. Issue 5 (1st August 2018)
- Main Title:
- Interleukin‐34, a comprehensive review
- Authors:
- Baghdadi, Muhammad
Umeyama, Yui
Hama, Naoki
Kobayashi, Takuto
Han, Nanumi
Wada, Haruka
Seino, Ken‐ichiro - Other Names:
- Yoshimura Akihiko guestEditor.
Iwakura Yoichiro guestEditor. - Abstract:
- Abstract: IL‐34 is a novel cytokine that was identified in 2008 in a comprehensive proteomic analysis as a tissue‐specific ligand of CSF‐1 receptor (CSF‐1R). IL‐34 exists in all vertebrates including fish, amphibians, birds, and mammals, showing high conservation among species. Structurally, IL‐34 belongs to the short‐chain helical hematopoietic cytokine family but shows no apparent consensus structural domains, motifs, or sequence homology with other cytokines. IL‐34 is synthesized as a secreted homodimeric glycoprotein that binds to the extracellular domains of CSF‐1R and receptor‐type protein‐tyrosine phosphatase‐zeta (PTP‐ζ) in addition to the chondroitin sulfate chains of syndecan‐1. These interactions result in activating several signaling pathways that regulate major cellular functions, including proliferation, differentiation, survival, metabolism, and cytokine/chemokine expression in addition to cellular adhesion and migration. In the steady state, IL‐34 contributes to the development and maintenance of specific myeloid cell subsets in a tissue‐specific manner: Langerhans cells in the skin and microglia in the brain. In pathological conditions, changes in IL‐34 expression—increased or decreased—are involved in disease pathogenesis and correlate with progression, severity, and chronicity. One decade after its discovery, IL‐34 has been introduced as a newcomer to the big family of interleukins with specific physiological functions, critical pathological roles, andAbstract: IL‐34 is a novel cytokine that was identified in 2008 in a comprehensive proteomic analysis as a tissue‐specific ligand of CSF‐1 receptor (CSF‐1R). IL‐34 exists in all vertebrates including fish, amphibians, birds, and mammals, showing high conservation among species. Structurally, IL‐34 belongs to the short‐chain helical hematopoietic cytokine family but shows no apparent consensus structural domains, motifs, or sequence homology with other cytokines. IL‐34 is synthesized as a secreted homodimeric glycoprotein that binds to the extracellular domains of CSF‐1R and receptor‐type protein‐tyrosine phosphatase‐zeta (PTP‐ζ) in addition to the chondroitin sulfate chains of syndecan‐1. These interactions result in activating several signaling pathways that regulate major cellular functions, including proliferation, differentiation, survival, metabolism, and cytokine/chemokine expression in addition to cellular adhesion and migration. In the steady state, IL‐34 contributes to the development and maintenance of specific myeloid cell subsets in a tissue‐specific manner: Langerhans cells in the skin and microglia in the brain. In pathological conditions, changes in IL‐34 expression—increased or decreased—are involved in disease pathogenesis and correlate with progression, severity, and chronicity. One decade after its discovery, IL‐34 has been introduced as a newcomer to the big family of interleukins with specific physiological functions, critical pathological roles, and promising clinical applications in disease diagnosis and treatment. In this review, we celebrate the 10th anniversary of IL‐34 discovery, introducing its biological characteristics, and discussing the importance of IL‐34 signaling network in health and disease. Abstract : IL‐34, a newcomer to the big family of interleukins with specific physiological functions and critical pathological roles. … (more)
- Is Part Of:
- Journal of leukocyte biology. Volume 104:Issue 5(2018)
- Journal:
- Journal of leukocyte biology
- Issue:
- Volume 104:Issue 5(2018)
- Issue Display:
- Volume 104, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 104
- Issue:
- 5
- Issue Sort Value:
- 2018-0104-0005-0000
- Page Start:
- 931
- Page End:
- 951
- Publication Date:
- 2018-08-01
- Subjects:
- CSF‐1R ligands -- cytokine -- development -- homeostasis -- immunity -- inflammation
Leucocytes -- Periodicals
Reticulo-endothelial system -- Periodicals
571.96 - Journal URLs:
- http://jlb.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1938-3673/ ↗
https://academic.oup.com/jleukbio ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/JLB.MR1117-457R ↗
- Languages:
- English
- ISSNs:
- 0741-5400
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5010.305000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8023.xml