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Open AccessJournal ArticleDOI

TGF-β1–Containing Exosomes from Injured Epithelial Cells Activate Fibroblasts to Initiate Tissue Regenerative Responses and Fibrosis

TLDR
It is suggested that TGF-β1 mRNA transported by exosomes constitutes a rapid response to initiate tissue repair/regenerative responses and activation of fibroblasts when resident parenchyma is injured.
Abstract
Hypoxia is associated with tissue injury and fibrosis but its functional role in fibroblast activation and tissue repair/regeneration is unknown. Using kidney injury as a model system, we demonstrate that injured epithelial cells produce an increased number of exosomes with defined genetic information to activate fibroblasts. Exosomes released by injured epithelial cells promote proliferation, α-smooth muscle actin expression, F-actin expression, and type I collagen production in fibroblasts. Fibroblast activation is dependent on exosomes delivering TGF-β1 mRNA among other yet to be identified moieties. This study suggests that TGF-β1 mRNA transported by exosomes constitutes a rapid response to initiate tissue repair/regenerative responses and activation of fibroblasts when resident parenchyma is injured. The results also inform potential utility of exosome-targeted therapies to control tissue fibrosis.

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The biology and function of fibroblasts in cancer

TL;DR: Cancer-associated fibroblasts (CAFs) become synthetic machines that produce many different tumour components and have a role in creating extracellular matrix structure and metabolic and immune reprogramming of the tumour microenvironment with an impact on adaptive resistance to chemotherapy.
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Overview of Extracellular Vesicles, Their Origin, Composition, Purpose, and Methods for Exosome Isolation and Analysis

TL;DR: The purpose of this review is to not only introduce the different types of extracellular vesicles but also to summarize their differences and similarities, and discuss different methods of exosome isolation and analysis currently used.
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Exosomes in Cancer Development, Metastasis and Drug Resistance: A Comprehensive Review

TL;DR: It is proposed that the successful combination of cancer treatments to tackle exosome-mediated drug resistance requires an interdisciplinary understanding of these cellular exclusion mechanisms, and how secreted biomolecules are involved in cellular cross-talk within the tumor microenvironment.
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Isolation of Extracellular Vesicles: General Methodologies and Latest Trends.

TL;DR: This review consolidates the data on the classical and state-of-the-art methods for isolation of EVs, including exosomes, highlighting the advantages and disadvantages of each method.
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Exosomes in tumor microenvironment influence cancer progression and metastasis

TL;DR: Different mechanisms associated with biogenesis, payload, and transport of exosomes are discussed, which may exert an immunosuppressive function as well as trigger an anti-tumor response by presenting tumor antigens to dendritic cells.
References
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Journal ArticleDOI

Myofibroblasts and mechano-regulation of connective tissue remodelling

TL;DR: It is clear that the understanding of the myofibroblast — its origins, functions and molecular regulation — will have a profound influence on the future effectiveness not only of tissue engineering but also of regenerative medicine generally.
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Prevalence of chronic kidney disease and decreased kidney function in the adult US population: Third national health and nutrition examination survey

TL;DR: CKD is common and warrants improved detection and classification using standardized criteria to improve outcomes, and CCr estimates showed a steeper decline with age and were lower in non-Hispanic blacks.
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Eradication of established murine tumors using a novel cell-free vaccine: dendritic cell-derived exosomes

TL;DR: Dendritic cells are shown to secrete antigen presenting vesicles, called exosomes, which express functional Major Histocompatibility Complex class I and class II, and T-cell costimulatory molecules, which prime specific cytotoxic T lymphocytes in vivo.
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Epithelial cell cycle arrest in G2/M mediates kidney fibrosis after injury.

TL;DR: In ischemic, toxic and obstructive models of AKI, it is demonstrated that treatment with a JNK inhibitor, or bypassing the G2/M arrest by administration of a p53 inhibitor or the removal of the contralateral kidney, rescues fibrosis in the unilateral isChemic injured kidney.
Journal ArticleDOI

Role of tissue stroma in cancer cell invasion.

TL;DR: A better understanding of stromal contributions to cancer progression will likely increase the awareness of the importance of the combinatorial signals that support and promote growth, dedifferentiation, invasion, and ectopic survival and eventually result in the identification of new therapeutics targeting the stroma.
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