Related Experiment Video
Updated: Oct 13, 2025

08:34
Precise Visualization of Insulin Receptors A and B in Murine Brain with an RNA In Situ Hybridization Assay
Published on: July 15, 2025
217
IL-34, the rationale for its expression in physiological and pathological conditions
Ryo Otsuka1, Haruka Wada1, Ken-Ichiro Seino1
1Institute for Genetic Medicine, Hokkaido University, Kita-15, Nishi-7, Sapporo, Hokkaido, 060-0815, Japan.
Seminars in Immunology
|November 14, 2021
Summary
Interleukin-34 (IL-34) binds to CSF-1 receptor, similar to CSF-1, but has distinct roles in disease. Understanding IL-34
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Interleukin-34 (IL-34) is a cytokine that binds to the colony-stimulating factor 1 receptor (CSF-1R).
- IL-34 shares CSF-1R with CSF-1, challenging previous notions of CSF-1R signaling.
- Other IL-34 receptors include protein-tyrosine phosphatase (PTP)-ζ and Syndecan-1.
Purpose of the Study:
- To comprehensively review the physiological and pathological roles of IL-34.
- To compare and contrast IL-34 with CSF-1 regarding receptor binding and downstream signaling.
- To explore the reasons behind IL-34's varied expression patterns in different diseases.
Main Methods:
- Literature review of existing studies on IL-34.
- Analysis of IL-34's interactions with CSF-1R, PTP-ζ, and Syndecan-1.
- Examination of IL-34's role in various diseases, including cancer, brain disorders, and dermal conditions.
Main Results:
- IL-34 and CSF-1 induce similar downstream signaling via CSF-1R, leading to distinct physiological outcomes.
- IL-34 is implicated in cancer progression and therapy resistance by promoting myeloid cell remodeling and reducing immunotherapy efficacy.
- IL-34 expression is downregulated in certain brain and dermal disorders.
Conclusions:
- IL-34 exhibits complex and context-dependent roles in human health and disease.
- Further research is needed to fully elucidate the multifaceted nature of IL-34.
- Targeting IL-34 may offer therapeutic potential in diseases where it plays a detrimental role.
Related Concept Videos
Regulation of the Unfolded Protein Response
2.7K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.7K
Regulation of Angiogenesis and Blood Supply
2.9K
Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits. Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.9K
MicroRNAs
3.2K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.2K

