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      In vitro Studies of Transendothelial Migration for Biological and Drug Discovery

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          Abstract

          Inflammatory diseases and cancer metastases lack concrete pharmaceuticals for their effective treatment despite great strides in advancing our understanding of disease progression. One feature of these disease pathogeneses that remains to be fully explored, both biologically and pharmaceutically, is the passage of cancer and immune cells from the blood to the underlying tissue in the process of extravasation. Regardless of migratory cell type, all steps in extravasation involve molecular interactions that serve as a rich landscape of targets for pharmaceutical inhibition or promotion. Transendothelial migration (TEM), or the migration of the cell through the vascular endothelium, is a particularly promising area of interest as it constitutes the final and most involved step in the extravasation cascade. While in vivo models of cancer metastasis and inflammatory diseases have contributed to our current understanding of TEM, the knowledge surrounding this phenomenon would be significantly lacking without the use of in vitro platforms. In addition to the ease of use, low cost, and high controllability, in vitro platforms permit the use of human cell lines to represent certain features of disease pathology better, as seen in the clinic. These benefits over traditional pre-clinical models for efficacy and toxicity testing are especially important in the modern pursuit of novel drug candidates. Here, we review the cellular and molecular events involved in leukocyte and cancer cell extravasation, with a keen focus on TEM, as discovered by seminal and progressive in vitro platforms. In vitro studies of TEM, specifically, showcase the great experimental progress at the lab bench and highlight the historical success of in vitro platforms for biological discovery. This success shows the potential for applying these platforms for pharmaceutical compound screening. In addition to immune and cancer cell TEM, we discuss the promise of hepatocyte transplantation, a process in which systemically delivered hepatocytes must transmigrate across the liver sinusoidal endothelium to successfully engraft and restore liver function. Lastly, we concisely summarize the evolving field of porous membranes for the study of TEM.

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          Most cited references181

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          New insights into the mechanisms of epithelial–mesenchymal transition and implications for cancer

          Epithelial-mesenchymal transition (EMT) is a cellular programme that is known to be crucial for embryogenesis, wound healing and malignant progression. During EMT, cell-cell and cell-extracellular matrix interactions are remodelled, which leads to the detachment of epithelial cells from each other and the underlying basement membrane, and a new transcriptional programme is activated to promote the mesenchymal fate. In the context of neoplasias, EMT confers on cancer cells increased tumour-initiating and metastatic potential and a greater resistance to elimination by several therapeutic regimens. In this Review, we discuss recent findings on the mechanisms and roles of EMT in normal and neoplastic tissues, and the cell-intrinsic signals that sustain expression of this programme. We also highlight how EMT gives rise to a variety of intermediate cell states between the epithelial and the mesenchymal state, which could function as cancer stem cells. In addition, we describe the contributions of the tumour microenvironment in inducing EMT and the effects of EMT on the immunobiology of carcinomas.
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            A perspective on cancer cell metastasis.

            Metastasis causes most cancer deaths, yet this process remains one of the most enigmatic aspects of the disease. Building on new mechanistic insights emerging from recent research, we offer our perspective on the metastatic process and reflect on possible paths of future exploration. We suggest that metastasis can be portrayed as a two-phase process: The first phase involves the physical translocation of a cancer cell to a distant organ, whereas the second encompasses the ability of the cancer cell to develop into a metastatic lesion at that distant site. Although much remains to be learned about the second phase, we feel that an understanding of the first phase is now within sight, due in part to a better understanding of how cancer cell behavior can be modified by a cell-biological program called the epithelial-to-mesenchymal transition.
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              Reconstituting organ-level lung functions on a chip.

              Here, we describe a biomimetic microsystem that reconstitutes the critical functional alveolar-capillary interface of the human lung. This bioinspired microdevice reproduces complex integrated organ-level responses to bacteria and inflammatory cytokines introduced into the alveolar space. In nanotoxicology studies, this lung mimic revealed that cyclic mechanical strain accentuates toxic and inflammatory responses of the lung to silica nanoparticles. Mechanical strain also enhances epithelial and endothelial uptake of nanoparticulates and stimulates their transport into the underlying microvascular channel. Similar effects of physiological breathing on nanoparticle absorption are observed in whole mouse lung. Mechanically active "organ-on-a-chip" microdevices that reconstitute tissue-tissue interfaces critical to organ function may therefore expand the capabilities of cell culture models and provide low-cost alternatives to animal and clinical studies for drug screening and toxicology applications.
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                Author and article information

                Contributors
                Journal
                Front Med Technol
                Front Med Technol
                Front. Med. Technol.
                Frontiers in Medical Technology
                Frontiers Media S.A.
                2673-3129
                16 November 2020
                2020
                : 2
                : 600616
                Affiliations
                [1] 1Biomedical Engineering, University of Rochester , Rochester, NY, United States
                [2] 2Biomedical Engineering, Rochester Institute of Technology , Rochester, NY, United States
                [3] 3Bioengineering, Clemson University , Clemson, SC, United States
                Author notes

                Edited by: Parveen Sharma, University of Liverpool, United Kingdom

                Reviewed by: Chris John Weston, University of Birmingham, United Kingdom; Weidong Zhao, China Medical University, China

                *Correspondence: James L. McGrath jmcgrath@ 123456bme.rochester.edu

                This article was submitted to Pharmaceutical Innovation, a section of the journal Frontiers in Medical Technology

                Article
                10.3389/fmedt.2020.600616
                8757899
                35047883
                a0de313f-b40b-4873-9bce-ddcd09596973
                Copyright © 2020 Salminen, Allahyari, Gholizadeh, McCloskey, Ajalik, Cottle, Gaborski and McGrath.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 30 August 2020
                : 20 October 2020
                Page count
                Figures: 4, Tables: 2, Equations: 0, References: 181, Pages: 19, Words: 16459
                Funding
                Funded by: National Institutes of Health, doi 10.13039/100000002;
                Award ID: 1422921
                Award ID: 5P20 GM103499-16
                Award ID: R35 GM119623-01
                Award ID: R43 GM137651-01
                Award ID: T32 HL066988
                Categories
                Medical Technology
                Review

                transendothelial migration,extravasation,leukocytes,metastasis,in vitro platforms,drug discovery,hepatocyte transplantation,porous membranes

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