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Updated: Jun 5, 2025

In Vitro Differentiation of Human Mesenchymal Stem Cells into Functional Cardiomyocyte-like Cells
Published on: August 9, 2017
Perspective: Pathological transdifferentiation-a novel therapeutic target for cardiovascular diseases and chronic
William Y Yang1, Mohammed Ben Issa1, Fatma Saaoud1
1Department of Cardiovascular Sciences, Lemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United States.
Abstract:
Pathological transdifferentiation, where differentiated cells aberrantly transform into other cell types that exacerbate disease rather than promote healing, represents a novel and significant concept. This perspective discusses its role and potential targeting in cardiovascular diseases and chronic inflammation. Current therapies mainly focus on mitigating early inflammatory response through proinflammatory cytokines and pathways targeting, including corticosteroids, TNF-α inhibitors, IL-1β monoclonal antibodies and blockers, IL-6 blockers, and nonsteroidal anti-inflammatory drugs (NSAIDs), along with modulating innate immune memory (trained immunity). However, these approaches often fail to address long-term tissue damage and functional regeneration. For instance, fibroblasts can transdifferentiate into myofibroblasts in cardiac fibrosis, and endothelial cells may undergo endothelial to mesenchymal transition (EndMT) in vascular remodeling, resulting in fibrosis and impaired tissue function. Targeting pathological transdifferentiation represents a promising therapeutic avenue by focusing on key signaling pathways that drive these aberrant cellular phenotypic and transcriptomic transitions. This approach seeks to inhibit these pathways or modulate cellular plasticity to promote effective tissue regeneration and prevent fibrosis. Such strategies have the potential to address inflammation, cell death, and the resulting tissue damage, providing a more comprehensive and sustainable treatment solution. Future research should focus on understanding the mechanisms behind pathological transdifferentiation, identifying relevant biomarkers and master regulators, and developing novel therapies through preclinical and clinical trials. Integrating these new therapies with existing anti-inflammatory treatments could enhance efficacy and improve patient outcomes. Highlighting pathological transdifferentiation as a therapeutic target could transform treatment paradigms, leading to better management and functional recovery of cardiovascular tissues in diseases and chronic inflammation.
Insights
Pathological transdifferentiation, a process where cells change type causing disease, is a new therapeutic target. Targeting this aberrant cell change offers a novel strategy for cardiovascular diseases and chronic inflammation, promoting tissue repair.
Area of Science:
- Cell Biology
- Pathology
- Immunology
Background:
- Pathological transdifferentiation involves differentiated cells changing type, worsening disease instead of healing.
- Current therapies target early inflammation but often fail to address long-term tissue damage and regeneration.
- Examples include fibroblast to myofibroblast transdifferentiation in cardiac fibrosis and endothelial-to-mesenchymal transition (EndMT) in vascular remodeling.
Purpose of the Study:
- To discuss the role of pathological transdifferentiation in cardiovascular diseases and chronic inflammation.
- To explore targeting pathological transdifferentiation as a novel therapeutic strategy.
- To highlight the potential for improved tissue regeneration and fibrosis prevention.
Main Methods:
- Review and perspective on existing literature regarding cellular transdifferentiation in disease.
- Analysis of current anti-inflammatory therapies and their limitations.
- Identification of signaling pathways driving aberrant cellular transitions.
Main Results:
- Pathological transdifferentiation contributes to fibrosis and impaired function in cardiovascular diseases and chronic inflammation.
- Targeting key signaling pathways offers a promising approach to inhibit aberrant cell transitions.
- Modulating cellular plasticity can promote effective tissue regeneration and prevent fibrosis.
Conclusions:
- Targeting pathological transdifferentiation presents a novel therapeutic avenue beyond current anti-inflammatory treatments.
- This strategy has the potential to address inflammation, cell death, and tissue damage comprehensively.
- Future research should focus on understanding mechanisms, identifying biomarkers, and developing targeted therapies for better patient outcomes.
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