Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. In Situ Quantification of Surface Chemistry in Porous Collagen Biomaterials

In Situ Quantification of Surface Chemistry in Porous Collagen Biomaterials

Thumbnail Image
Download
Name

10439_2015_Article_1445.pdf

Size

2.72 MB

Format

Adobe PDF

Checksum (MD5)

f1d56c17e8b53a381b86988f61f774cf

Download all files submitted through automated deposit
art_8712534945951169975.zip (2.21 MB)
Author(s)
Tzeranis, Dimitrios
•
Soller, Eric Charles
•
Buydash, Melissa Christine
•
So, Peter T. C.
•
Yannas, Ioannis V
Date Issued
September 2015
Journal
Annals of Biomedical Engineering
Publisher
Springer US
Citation
Tzeranis, Dimitrios S. et al. “In Situ Quantification of Surface Chemistry in Porous Collagen Biomaterials.” Annals of Biomedical Engineering 44.3 (2016): 803–815.
Version
Author's final manuscript
Abstract
Cells inside a 3D matrix (such as tissue extracellular matrix or biomaterials) sense their insoluble environment through specific binding interactions between their adhesion receptors and ligands present on the matrix surface. Despite the critical role of the insoluble matrix in cell regulation, there exist no widely-applicable methods for quantifying the chemical stimuli provided by a matrix to cells. Here, we describe a general-purpose technique for quantifying in situ the density of ligands for specific cell adhesion receptors of interest on the surface of a 3D matrix. This paper improves significantly the accuracy of the procedure introduced in a previous publication by detailed marker characterization, optimized staining, and improved data interpretation. The optimized methodology is utilized to quantify the ligands of integrins α[subscript 1]β[subscript 1], α[subscript 2]β[subscript 1] on two kinds of matched porous collagen scaffolds, which are shown to possess significantly different ligand density, and significantly different ability to induce peripheral nerve regeneration in vivo. Data support the hypothesis that cell adhesion regulates contractile cell phenotypes, recently shown to be inversely related to organ regeneration. The technique provides a standardized way to quantify the surface chemistry of 3D matrices, and a means for introducing matrix effects in quantitative biological models.
MIT Department
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Department of Mechanical Engineering
Terms of Use
Creative Commons Attribution-Noncommercial-Share Alike
http://creativecommons.org/licenses/by-nc-sa/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/105254
DOI of Published Version
https://doi.org/10.1007/s10439-015-1445-x
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.