Format

Send to

Choose Destination
Tissue Eng Part A. 2016 Oct;22(19-20):1204-1217. Epub 2016 Sep 29.

Human Corneal Fibroblast Pattern Evolution and Matrix Synthesis on Mechanically Biased Substrates.

Author information

1
1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.
2
2 Department of Electrical and Computer Engineering, Northeastern University , Boston, Massachusetts.
3
3 The Institute of Photonic Sciences , Castelldefels (Barcelona), Spain .
4
4 Department of Ophthalmology, Dean McGee Eye Institute, Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
5
5 Departments of Mechanical Engineering and Department of Pharmacology and Center for Lung Biology, University of South Alabama , Mobile, Alabama.
6
6 Department of Surgery, Harvard Medical School , Boston, Massachusetts.
7
7 Schepens Eye Research Institute , Boston, Massachusetts.

Abstract

In a fibroblast colony model of corneal stromal development, we asked how physiological tension influences the patterning dynamics of fibroblasts and the orientation of deposited extracellular matrix (ECM). Using long-term live-cell microscopy, enabled by an optically accessible mechanobioreactor, a primary human corneal fibroblast colony was cultured on three types of substrates: a mechanically biased, loaded, dense, disorganized collagen substrate (LDDCS), a glass coverslip, and an unloaded, dense, disorganized collagen substrate (UDDCS). On LDDCS, fibroblast orientation and migration along a preferred angle developed early, cell orientation was correlated over long distances, and the colony pattern was stable. On glass, fibroblast orientation was poorly correlated, developed more slowly, and colony patterns were metastable. On UDDCS, cell orientation was correlated over shorter distances compared with LDDCS specimens. On all substrates, the ECM pattern reflected the cell pattern. In summary, mechanically biasing the collagen substrate altered the early migration behavior of individual cells, leading to stable emergent cell patterning, which set the template for newly synthesized ECM.

PMID:
27600605
PMCID:
PMC5073220
DOI:
10.1089/ten.TEA.2016.0164
[Indexed for MEDLINE]
Free PMC Article

Conflict of interest statement

Disclosure StatementThe custom mechanobioreactor used in this investigation has now been commercialized by Admet Corporation under the name BioTense®. However, no authors benefit financially from the commercialization agreement. Thus, no competing financial interests exist.

Supplemental Content

Full text links

Icon for Atypon Icon for PubMed Central
Loading ...
Support Center