4.6 Review

Stem Cell Based Approaches to Modulate the Matrix Milieu in Vascular Disorders

Journal

FRONTIERS IN CARDIOVASCULAR MEDICINE
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcvm.2022.879977

Keywords

ECM; regenerative repair; cardiovascular; elastin; collagen; exosomes

Funding

  1. National Institutes of Health (NHLBI) [HL 139662-01]
  2. National Science Foundation [CBET 1926939]
  3. American Heart Association [19TPA34890029]
  4. Lehigh University usable to cover publishing costs

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The extracellular matrix (ECM) plays a crucial role in maintaining the structure and function of vascular tissues. Changes in the ECM microenvironment can lead to altered tissue function and exacerbation of vascular pathologies. Stem cell (SC)-based therapies hold potential for ECM repair, but face challenges in cell processing, delivery, and maintaining phenotypic integrity.
The extracellular matrix (ECM) represents a complex and dynamic framework for cells, characterized by tissue-specific biophysical, mechanical, and biochemical properties. ECM components in vascular tissues provide structural support to vascular cells and modulate their function through interaction with specific cell-surface receptors. ECM-cell interactions, together with neurotransmitters, cytokines, hormones and mechanical forces imposed by blood flow, modulate the structural organization of the vascular wall. Changes in the ECM microenvironment, as in post-injury degradation or remodeling, lead to both altered tissue function and exacerbation of vascular pathologies. Regeneration and repair of the ECM are thus critical toward reinstating vascular homeostasis. The self-renewal and transdifferentiating potential of stem cells (SCs) into other cell lineages represents a potentially useful approach in regenerative medicine, and SC-based approaches hold great promise in the development of novel therapeutics toward ECM repair. Certain adult SCs, including mesenchymal stem cells (MSCs), possess a broader plasticity and differentiation potential, and thus represent a viable option for SC-based therapeutics. However, there are significant challenges to SC therapies including, but not limited to cell processing and scaleup, quality control, phenotypic integrity in a disease milieu in vivo, and inefficient delivery to the site of tissue injury. SC-derived or -inspired strategies as a putative surrogate for conventional cell therapy are thus gaining momentum. In this article, we review current knowledge on the patho-mechanistic roles of ECM components in common vascular disorders and the prospects of developing adult SC based/inspired therapies to modulate the vascular tissue environment and reinstate vessel homeostasis in these disorders.

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