Published April 2013 | Version v1
Journal article

Rigid microenvironments promote cardiac differentiation of mouse and human embryonic stem cells

  • 1. Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90095 (United States)
  • 2. Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095 (United States)
  • 3. Department of Orthopaedic Surgery, University of California, Los Angeles, CA 90095 (United States)
  • 4. California NanoSystems Institute, University of California, Los Angeles, CA 90095 (United States)

Description

While adult heart muscle is the least regenerative of tissues, embryonic cardiomyocytes are proliferative, with embryonic stem (ES) cells providing an endless reservoir. In addition to secreted factors and cell–cell interactions, the extracellular microenvironment has been shown to play an important role in stem cell lineage specification, and understanding how scaffold elasticity influences cardiac differentiation is crucial to cardiac tissue engineering. Though previous studies have analyzed the role of matrix elasticity on the function of differentiated cardiomyocytes, whether it affects the induction of cardiomyocytes from pluripotent stem cells is poorly understood. Here, we examine the role of matrix rigidity on cardiac differentiation using mouse and human ES cells. Culture on polydimethylsiloxane (PDMS) substrates of varied monomer-to-crosslinker ratios revealed that rigid extracellular matrices promote a higher yield of de novo cardiomyocytes from undifferentiated ES cells. Using a genetically modified ES system that allows us to purify differentiated cardiomyocytes by drug selection, we demonstrate that rigid environments induce higher cardiac troponin T expression, beating rate of foci, and expression ratio of adult α- to fetal β- myosin heavy chain in a purified cardiac population. M-mode and mechanical interferometry image analyses demonstrate that these ES-derived cardiomyocytes display functional maturity and synchronization of beating when co-cultured with neonatal cardiomyocytes harvested from a developing embryo. Together, these data identify matrix stiffness as an independent factor that instructs not only the maturation of already differentiated cardiomyocytes but also the induction and proliferation of cardiomyocytes from undifferentiated progenitors. Manipulation of the stiffness will help direct the production of functional cardiomyocytes en masse from stem cells for regenerative medicine purposes. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1468-6996/14/2/025003

Additional details

Publishing Information

Journal Title
Science and Technology of Advanced Materials
Journal Volume
14
Journal Issue
2
Journal Page Range
[8 p.]
ISSN
1468-6996

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
44061316
Subject category
S60: APPLIED LIFE SCIENCES; S36: MATERIALS SCIENCE;
Descriptors DEI
ADULTS; CELL CULTURES; ELASTICITY; EMBRYOS; FLEXIBILITY; INTERACTIONS; INTERFEROMETRY; MICE; MONOMERS; MYOSIN; STEM CELLS; SUBSTRATES
Descriptors DEC
AGE GROUPS; ANIMAL CELLS; ANIMALS; GLOBULINS; MAMMALS; MECHANICAL PROPERTIES; ORGANIC COMPOUNDS; PROTEINS; RODENTS; SOMATIC CELLS; TENSILE PROPERTIES; VERTEBRATES