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Author Spotlight: Advancing the Analysis of Plasma Extracellular Vesicle Proteome for Cardiovascular Biomarker Studies
Published on: January 31, 2025
Identifying Plasma Derived Extracellular Vesicle (EV) Contained Biomarkers in the Development of Chronic Neuropathic
Natasha M Sosanya1, Raina Kumar2, John L Clifford3
1United States Army Institute of Surgical Research, Fort Sam Houston, San Antonio, Texas.
Abstract:
Research into potentially novel biomarkers for chronic pain development is lacking. microRNAs (miRNAs) are attractive candidates as biomarkers due to their conservation across species, stability in liquid biopsies, and variation that corresponds to a pathologic state. miRNAs can be sorted into extracellular vesicles (EVs) within the cell and released from the site of injury. EVs transfer cargo molecules between cells thus affecting key intercellular signaling pathways. The focus of this study was to determine the plasma derived EV miRNA content in a chronic neuropathic pain rat model. This was accomplished by performing either spinal nerve ligation (SNL; n = 6) or sham (n = 6) surgery on anesthetized male Sprague-Dawley rats. Mechanosensitivity was assessed and plasma derived EV RNA was isolated at baseline (BL), day 3, and 15 postnerve injury. EV extracted small RNA was sequenced followed by differentially expressed (DE) miRNAs and gene target enrichment/signaling pathway analysis performed using R packages and TargetScan/Ingenuity pathway analysis (IPA), respectively. Seven of the DE miRNAs were validated by Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR). The data indicated that SNL rats displayed a time-dependent threshold reduction in response to evoked stimuli from day 3 to day 15 postnerve injury. The data also revealed that 22 and 74 miRNAs at day 3 and 15, respectively, and 33 miRNAs at both day 3 and 15 were uniquely DE between the SNL and sham groups. The key findings from this proposal include (1) the majority of the DE EV miRNAs, which normally function to suppress inflammation, were downregulated, and (2) several of the plasma derived DE EV miRNAs reflect previously observed changes in the injured L5 nerve. The plasma derived DE EV miRNAs regulate processes important in the development and maintenance of neuropathic pain states and potentially serve as key regulators, biomarkers, and targets in the progression and treatment of chronic neuropathic pain. PERSPECTIVE: This article describes the DE miRNA content of plasma derived EVs, comparing neuropathic pain to normal conditions. This data indicates that EV miRNAs may be important in nociception and may also serve as biomarkers for chronic pain. These results encourage further research on EV miRNAs in chronic neuropathic pain sufferers.
Insights
Researchers identified specific microRNAs (miRNAs) within extracellular vesicles (EVs) in the blood of rats with chronic neuropathic pain. These EV miRNAs, altered during pain development, show potential as biomarkers for diagnosing and treating chronic pain conditions.
Area of Science:
- Biomarker Discovery
- Neuroscience
- Molecular Biology
Background:
- Chronic pain lacks effective biomarkers.
- MicroRNAs (miRNAs) are stable molecules in liquid biopsies and can indicate disease states.
- Extracellular vesicles (EVs) transport miRNAs between cells, influencing intercellular signaling.
Purpose of the Study:
- To investigate plasma-derived EV miRNA profiles in a rat model of chronic neuropathic pain.
- To identify differentially expressed miRNAs associated with neuropathic pain development.
- To explore the potential of these miRNAs as biomarkers and therapeutic targets.
Main Methods:
- Spinal nerve ligation (SNL) surgery in rats to induce neuropathic pain.
- Isolation of plasma-derived EVs and extraction of small RNA.
- Next-generation sequencing of small RNA to identify differentially expressed miRNAs (DE miRNAs).
- Validation of selected DE miRNAs using Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR).
Main Results:
- SNL rats showed reduced mechanosensitivity from day 3 to day 15 post-injury.
- A significant number of DE miRNAs were identified in plasma EVs at day 3 and day 15 post-SNL.
- The majority of downregulated DE miRNAs normally suppress inflammation.
- Changes in plasma EV miRNAs mirrored alterations observed in the injured nerve.
Conclusions:
- Plasma-derived EV miRNAs are significantly altered in chronic neuropathic pain.
- These altered miRNAs play roles in pain development and maintenance.
- EV miRNAs represent promising biomarkers and potential therapeutic targets for chronic neuropathic pain.
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