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EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration

1
Schepens Eye Research Institute of Massachusetts Eye and Ear, Boston, MA 02114, USA
2
Department of Ophthalmology, Harvard Medical School, Boston, MA 02114, USA
3
Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(12), 4271; https://doi.org/10.3390/ijms21124271
Received: 1 June 2020 / Revised: 12 June 2020 / Accepted: 14 June 2020 / Published: 16 June 2020
(This article belongs to the Special Issue Molecular Biology of Age-Related Macular Degeneration (AMD) 2.0)
Epithelial–mesenchymal transition (EMT) and endothelial–mesenchymal transition (EndMT) are physiological processes required for normal embryogenesis. However, these processes can be hijacked in pathological conditions to facilitate tissue fibrosis and cancer metastasis. In the eye, EMT and EndMT play key roles in the pathogenesis of subretinal fibrosis, the end-stage of age-related macular degeneration (AMD) that leads to profound and permanent vision loss. Predominant in subretinal fibrotic lesions are matrix-producing mesenchymal cells believed to originate from the retinal pigment epithelium (RPE) and/or choroidal endothelial cells (CECs) through EMT and EndMT, respectively. Recent evidence suggests that EMT of RPE may also be implicated during the early stages of AMD. Transforming growth factor-beta (TGFβ) is a key cytokine orchestrating both EMT and EndMT. Investigations in the molecular mechanisms underpinning EMT and EndMT in AMD have implicated a myriad of contributing factors including signaling pathways, extracellular matrix remodelling, oxidative stress, inflammation, autophagy, metabolism and mitochondrial dysfunction. Questions arise as to differences in the mesenchymal cells derived from these two processes and their distinct mechanistic contributions to the pathogenesis of AMD. Detailed discussion on the AMD microenvironment highlights the synergistic interactions between RPE and CECs that may augment the EMT and EndMT processes in vivo. Understanding the differential regulatory networks of EMT and EndMT and their contributions to both the dry and wet forms of AMD can aid the development of therapeutic strategies targeting both RPE and CECs to potentially reverse the aberrant cellular transdifferentiation processes, regenerate the retina and thus restore vision. View Full-Text
Keywords: age-related macular degeneration; epithelial–mesenchymal transition; endothelial–mesenchymal transition; subretinal fibrosis; transforming growth factor-beta age-related macular degeneration; epithelial–mesenchymal transition; endothelial–mesenchymal transition; subretinal fibrosis; transforming growth factor-beta
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MDPI and ACS Style

Shu, D.Y.; Butcher, E.; Saint-Geniez, M. EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration. Int. J. Mol. Sci. 2020, 21, 4271. https://doi.org/10.3390/ijms21124271

AMA Style

Shu DY, Butcher E, Saint-Geniez M. EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration. International Journal of Molecular Sciences. 2020; 21(12):4271. https://doi.org/10.3390/ijms21124271

Chicago/Turabian Style

Shu, Daisy Y., Erik Butcher, and Magali Saint-Geniez. 2020. "EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration" International Journal of Molecular Sciences 21, no. 12: 4271. https://doi.org/10.3390/ijms21124271

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