Engineered N-cadherin substrates for stem cell differentiation

Qin, Ellen C.

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https://hdl.handle.net/2142/92878 Copy

Description

Title

Engineered N-cadherin substrates for stem cell differentiation

Author(s)

Qin, Ellen C.

Issue Date

2016-07-22

Director of Research (if dissertation) or Advisor (if thesis)

• Kong, Hyunjoon
• Leckband, Deborah E.

Department of Study

Chemical & Biomolecular Engr

Discipline

Chemical Engineering

Degree Granting Institution

University of Illinois at Urbana-Champaign

Degree Name

M.S.

Degree Level

Thesis

Keyword(s)

• N-cadherin
• Hydrogel
• Stiffness
• Bone marrow stromal cell

Abstract

In the case of injury, aging, or disease, tissues in the body may have a limited capability to regenerate. As a result, great interest have been put into tissue engineering as a way to assemble functional constructs that restore, maintain, or improve those tissues. Certain success was made to modulate neural differentiation of stem cells using soluble factors and cell adhesion matrix properties. These differentiation studies are often dependent on the density of cells plated on the substrate, which implies that there is an important role of cadherin-modulated cell-cell adhesion in regulating stem cell differentiation levels. As a result, the goal for this research is to develop a hydrogel platform which integrates the effects of N-cadherin and matrix stiffness to modulate cell differentiation. To create this system, Fc-tagged N-cadherins are attached to alginate gels of varying stiffness through Protein A, which is chemically bound to the surface. Different cells known to express N-cadherin were seeded onto the gels, with the bone marrow stromal cells (BMSCs) showing the best adhesion properties. This study thus demonstrates that N-cadherin substrates can be used to promote cell adhesion, and may be useful for differentiation studies with BMSCs.

Graduation Semester

2016-08

Type of Resource

text

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http://hdl.handle.net/2142/92878

Copyright and License Information

Copyright 2016 Ellen Qin

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