Abstract

Extracellular vesicles (EVs) are membrane enclosed micro- and nano-sized vesicles that are secreted from almost every species, ranging from prokaryotes to eukaryotes, and from almost every cell type studied so far. EVs contain repertoire of bioactive molecules such as proteins (including enzymes and transcriptional factors), lipids, carbohydrates and nucleic acids including DNA, coding and non-coding RNAs. The secreted EVs are taken up by neighboring cells where they release their content in recipient cells, or can sail through body fluids to reach distant organs. Since EVs transport bioactive cargo between cells, they have emerged as novel mediators of extra- and intercellular activities in local microenvironment and inter-organ communications distantly. Herein, we review the activities of EV-associated matrix-remodeling enzymes such as matrix metalloproteinases, heparanases, hyaluronidases, aggrecanases, and their regulators such as extracellular matrix metalloproteinase inducers and tissue inhibitors of metalloproteinases as novel means of matrix remodeling in physiological and pathological conditions. We discuss how such EVs act as novel mediators of extracellular matrix degradation to prepare a permissive environment for various pathological conditions such as cancer, cardiovascular diseases, arthritis and metabolic diseases. Additionally, the roles of EV-mediated matrix remodeling in tissue repair and their potential applications as organ therapies have been reviewed. Collectively, this knowledge could benefit the development of new approaches for tissue engineering.

Highlights

  • Extracellular matrix (ECM) provides mechanical and chemical support to cells and orchestrates the structural framework and homeostasis of connective tissues where the local components and composition of ECM collectively determine the biochemical properties of the connective tissue [1,2,3].The composition of ECM varies among multicellular structures whereby fibroblasts and epithelial cells are the most common cell types in the stromal architecture

  • It has been reported that Extracellular vesicles (EVs) isolated from ascites and sera of ovarian carcinoma patients containing matrix metalloproteinases (MMPs)-2, MMP-9 and plasmin are capable of promoting proteinase-dependent metastatic activity in malignant ovarian epithelium, indicating their diagnostic value [92]

  • The participation of EVs in the development of various diseases and tissue repair has well been elaborated for their nucleic acid and proteomic contents

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Summary

Introduction

Extracellular matrix (ECM) provides mechanical and chemical support to cells and orchestrates the structural framework and homeostasis of connective tissues where the local components and composition of ECM collectively determine the biochemical properties of the connective tissue [1,2,3]. In addition to physical contacts, the acellular or paracrine components of ECM, which include cell-derived secretome such as secreted soluble proteins, growth factors, cytokines and chemokines, facilitate the paracrine functional coordination in a structural framework of a connective tissue. One of the most profound characteristics of EVs that have been widely reported is their participation in intercellular communication by transporting molecules and transmitting biological messages between cells and play physiological roles [27]. Due to their abilities of transporting bioactive molecules and pathological signals, EVs actively participate in the progression of various diseases. The presence of proteolytic molecules in EVs is one of the newly discovered sources for tissue remodeling through pericellular gelatinolytic activities (proteolysis), which modulate the structural architecture and dynamics of ECM and contribute for both the development of various diseases, tissue regeneration and amelioration of organ functions that will be discussed in this review

MMPs Secretion into EVs
EV-Mediated
Construction of Pre-Metastatic Niche
Fibroblastic Switching and Acquisition of Mesenchymal Mode
Tumor Neovascularization
EV-Associated MMPs as Cancer Biomarkers
EV-Driven Matrix Destruction and Development of Arthritic Diseases
EV-Associated MMPs
EV-Driven Matrix Remodeling
Joint Repair
Cardiac Repair
Cutaneous Repair and Healing of Wounds
10. Concluding Remarks
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