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Updated: Jun 13, 2025

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
Published on: November 11, 2014
Oncostatin M receptor-dependent signaling assessed by RNA sequencing in mouse hematopoietic stem cells
Logan S Schwartz1,2, Ruth L Saxl1, Tim Stearns1
1The Jackson Laboratory, Bar Harbor, ME, USA.
Abstract:
Oncostatin M (OSM) is a member of the interleukin-6 (IL-6) family of cytokines and has been found to have anti-inflammatory and pro-inflammatory properties in various cellular and disease contexts. OSM signals through two receptor complexes, one of which includes OSMRβ. Here, we investigated OSM-OSMRβ signaling in adult mouse hematopoietic stem cells (HSCs) using the conditional Osmrfl/fl mouse model B6;129-Osmrtm1.1Nat/J. We crossed Osmrfl/fl mice to interferon-inducible Mx1-Cre, which is robustly induced in adult HSCs. From these mice, we isolated HSCs by flow cytometry, stimulated with recombinant OSM or vehicle for 1 hour, and assessed gene expression changes in control versus Osmr knockout HSCs by RNA-seq. This data may be utilized to investigate OSMRβ -dependent and -independent OSM signaling as well as the transcriptional effects of an IL-6 family cytokine on mouse HSCs to further define its anti-inflammatory versus pro-inflammatory properties.
Insights
Oncostatin M (OSM) signaling via OSMRβ impacts adult mouse hematopoietic stem cells (HSCs). This study defines OSM
Area of Science:
- Immunology
- Hematology
- Molecular Biology
Background:
- Oncostatin M (OSM), an IL-6 family cytokine, exhibits dual anti-inflammatory and pro-inflammatory roles.
- OSM signaling involves receptor complexes, including the OSM receptor subunit beta (OSMRβ).
- Understanding OSM's function in hematopoietic stem cells (HSCs) is crucial for immune and blood disorders.
Purpose of the Study:
- To investigate the role of OSMRβ-dependent OSM signaling in adult mouse HSCs.
- To elucidate the transcriptional effects of OSM on HSCs.
- To differentiate the anti-inflammatory versus pro-inflammatory properties of OSM in HSCs.
Main Methods:
- Utilized a conditional Osmr knockout mouse model (Osmrfl/fl crossed with Mx1-Cre).
- Isolated adult HSCs via flow cytometry.
- Stimulated HSCs with recombinant OSM and analyzed gene expression changes using RNA-sequencing.
Main Results:
- Identified gene expression alterations in HSCs following OSM stimulation.
- Compared transcriptional profiles between control and Osmr knockout HSCs.
- Provided data to distinguish OSMRβ-dependent and -independent OSM signaling pathways.
Conclusions:
- The study provides insights into OSM's molecular effects on HSCs.
- Findings contribute to understanding OSM's context-dependent inflammatory roles.
- Data can inform future research on cytokine signaling in hematopoiesis.
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