Hybrid live cell–supported membrane interfaces for signaling studies

A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development...

Full description

Saved in:
Bibliographic Details
Main Authors: Biswas, Kabir H., Groves, Jay T.
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2019
Subjects:
Online Access:https://hdl.handle.net/10356/104630
http://hdl.handle.net/10220/49522
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-104630
record_format dspace
spelling sg-ntu-dr.10356-1046302020-06-01T10:13:43Z Hybrid live cell–supported membrane interfaces for signaling studies Biswas, Kabir H. Groves, Jay T. School of Materials Science & Engineering NTU Institute for Health Technologies Receptor Clustering Cell Adhesion Receptor Engineering::Materials A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development of mechanical forces in cells. Unlike traditional experimental approaches, hybrid live cell–supported lipid bilayer (SLB) systems, wherein a live cell interacts with a synthetic substrate supported membrane, allow interrogation of these aspects of receptor signaling. The SLB system directly offers facile control over the identity, density, and mobility of ligands used for engaging cellular receptors. Further, application of various nano- and micropatterning techniques allows for spatial patterning of ligands. In this review, we describe the hybrid live cell–SLB system and its application in uncovering a range of spatial and mechanical aspects of receptor signaling. We highlight the T cell immunological synapse, junctions formed between EphA2- and ephrinA1-expressing cells, and adhesions formed by cadherin and integrin receptors. 2019-08-05T01:52:26Z 2019-12-06T21:36:32Z 2019-08-05T01:52:26Z 2019-12-06T21:36:32Z 2019 Journal Article Biswas, K. H., & Groves, J. T. (2019). Hybrid live cell–supported membrane interfaces for signaling studies. Annual Review of Biophysics, 48, 537-562. doi:10.1146/annurev-biophys-070317-033330 1936-122X https://hdl.handle.net/10356/104630 http://hdl.handle.net/10220/49522 10.1146/annurev-biophys-070317-033330 en Annual Review of Biophysics © 2019 Annual Reviews, Inc. All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Receptor Clustering
Cell Adhesion Receptor
Engineering::Materials
spellingShingle Receptor Clustering
Cell Adhesion Receptor
Engineering::Materials
Biswas, Kabir H.
Groves, Jay T.
Hybrid live cell–supported membrane interfaces for signaling studies
description A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development of mechanical forces in cells. Unlike traditional experimental approaches, hybrid live cell–supported lipid bilayer (SLB) systems, wherein a live cell interacts with a synthetic substrate supported membrane, allow interrogation of these aspects of receptor signaling. The SLB system directly offers facile control over the identity, density, and mobility of ligands used for engaging cellular receptors. Further, application of various nano- and micropatterning techniques allows for spatial patterning of ligands. In this review, we describe the hybrid live cell–SLB system and its application in uncovering a range of spatial and mechanical aspects of receptor signaling. We highlight the T cell immunological synapse, junctions formed between EphA2- and ephrinA1-expressing cells, and adhesions formed by cadherin and integrin receptors.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Biswas, Kabir H.
Groves, Jay T.
format Article
author Biswas, Kabir H.
Groves, Jay T.
author_sort Biswas, Kabir H.
title Hybrid live cell–supported membrane interfaces for signaling studies
title_short Hybrid live cell–supported membrane interfaces for signaling studies
title_full Hybrid live cell–supported membrane interfaces for signaling studies
title_fullStr Hybrid live cell–supported membrane interfaces for signaling studies
title_full_unstemmed Hybrid live cell–supported membrane interfaces for signaling studies
title_sort hybrid live cell–supported membrane interfaces for signaling studies
publishDate 2019
url https://hdl.handle.net/10356/104630
http://hdl.handle.net/10220/49522
_version_ 1681056644852613120