Open Research Newcastle
Browse

Identification of the microRNA networks contributing to macrophage differentiation and function

Download (3.71 MB)
journal contribution
posted on 2025-05-09, 13:03 authored by Hong Zhou, Jie Zhang, Fiona Eyers, Yang Xiang, Cristan Herbert, Hock L. Tay, Paul S. Foster, Ming YangMing Yang
Limited evidence is available about the specific miRNA networks that regulate differentiation of specific immune cells. In this study, we characterized miRNA expression and associated alterations in expression with putative mRNA targets that are critical during differentiation of macrophages. In an effort to map the dynamic changes in the bone marrow (BM), we profiled whole BM cultures during differentiation into macrophages. We identified 112 miRNAs with expression patterns that were differentially regulated 5-fold or more during BMDM development. With TargetScan and MeSH databases, we identified 1267 transcripts involved in 30 canonical pathways linked to macrophage biology as potentially regulated by these specific 112 miRNAs. Furthermore, by employing miRanda and Ingenuity Pathways Analysis (IPA) analysis systems, we identified 18 miRNAs that are temporally linked to the expression of CSF1R, CD36, MSR1 and SCARB1; 7 miRNAs linked to the regulation of the transcription factors RUNX1 and PU.1, and 14 miRNAs target the nuclear receptor PPARα and PPARγ. This novel information provides an important reference resource for further study of the functional links between miRNAs and their target mRNAs for the regulation of differentiation and function of macrophages.

History

Journal title

Oncotarget

Volume

7

Issue

20

Pagination

28806-28820

Publisher

Impact Journals LLC

Language

  • en, English

College/Research Centre

Faculty of Health and Medicine

School

School of Biomedical Sciences and Pharmacy

Rights statement

© 2016. This manuscript version is made available under the CC-BY-NC-ND 3.0 license https://creativecommons.org/licenses/by-nc-nd/3.0/.

Usage metrics

    Publications

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC