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Bioengineering
Desarrollo de tejido cardíaco humano organizado en 3D dentro de una plataforma microfluídica
Desarrollo de tejido cardíaco humano organizado en 3D dentro de una plataforma microfluídica
JoVE Journal
Bioengineering
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JoVE Journal Bioengineering
Developing 3D Organized Human Cardiac Tissue within a Microfluidic Platform

Desarrollo de tejido cardíaco humano organizado en 3D dentro de una plataforma microfluídica

Full Text
5,653 Views
10:42 min
June 15, 2021

DOI: 10.3791/62539-v

Jaimeson Veldhuizen1, Mehdi Nikkhah1,2

1School of Biological and Health Systems Engineering,Arizona State University, 2Biodesign Virginia G. Piper Center for Personalized Diagnostics,Arizona State University

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This protocol describes the development of a three-dimensional (3D) microfluidic model of human cardiac tissue. The model consists of stem cell-derived cardiomyocytes co-cultured with cardiac fibroblasts in a collagen-based hydrogel, aimed at enhancing cardiac tissue engineering and drug screening.

Key Study Components

Area of Science

  • Cardiac tissue engineering
  • Stem cell biology
  • Microfluidics

Background

  • Cardiovascular disease is the leading cause of death globally.
  • Traditional in vitro models often use monolayer cultures.
  • The myocardium's complexity necessitates more sophisticated models.
  • 3D models can better mimic the heart's cellular composition and structure.

Purpose of Study

  • To develop a 3D model of human cardiac tissue.
  • To improve the representation of cardiac tissue in vitro.
  • To facilitate applications in drug screening and disease modeling.

Methods Used

  • Development of a microfluidic device.
  • Creation of a 3D main tissue channel.
  • Incorporation of elliptical microposts for cell alignment.
  • Co-culture of cardiomyocytes and cardiac fibroblasts in hydrogel.

Main Results

  • Successful development of aligned human cardiac tissue.
  • Enhanced structural and functional properties of the tissue model.
  • Demonstrated potential for improved drug screening.
  • Provided insights into cardiac disease modeling.

Conclusions

  • The 3D microfluidic model effectively mimics human cardiac tissue.
  • This approach can advance research in cardiac health and disease.
  • Future applications may include personalized medicine and therapeutic testing.

Frequently Asked Questions

What is the significance of using a 3D model?
3D models better replicate the complex architecture and cellular interactions of actual tissues, leading to more accurate research outcomes.
How does the microfluidic device enhance the model?
The microfluidic device allows for precise control of the cellular environment, promoting better alignment and functionality of cardiac cells.
What are the potential applications of this research?
This research can be applied in drug screening, disease modeling, and understanding cardiac tissue responses to various stimuli.
What types of cells are used in the model?
The model uses stem cell-derived cardiomyocytes and cardiac fibroblasts.
Why is alignment of cardiac cells important?
Cell alignment is crucial for mimicking the natural structure of heart tissue, which is essential for proper function and response to treatments.
Can this model be used for studying other diseases?
While focused on cardiac tissue, the principles of this model may be adapted for studying other diseases involving complex tissue structures.

El objetivo de este protocolo es explicar y demostrar el desarrollo de un modelo microfluídico tridimensional (3D) de tejido cardíaco humano altamente alineado, compuesto por cardiomiocitos derivados de células madre co-cultivados con fibroblastos cardíacos (CF) dentro de un hidrogel biomimético a base de colágeno, para aplicaciones en ingeniería de tejido cardíaco, detección de fármacos y modelado de enfermedades.

Las enfermedades cardiovasculares siguen siendo la primera causa de muerte en todo el mundo. Los modelos in vitro tradicionales se basan en el cultivo monocapa. Sin embargo, el corazón, específicamente el músculo cardíaco o el miocardio, es complejo en su anisotropía 3D y composición celular.

Por lo tanto, es crítico mejorar la complejidad de la composición del tejido dentro de modelos ines vitro para imitar mejor los componentes celulares y la estructura del miocardio. Aquí en este trabajo, demostramos un protocolo para el desarrollo de un tejido cardíaco humano derivado de células madre maduras 3D dentro de un nuevo dispositivo microfluídico. Este dispositivo incorpora un canal de tejido principal 3D con microposts elípticos innatos que inducen altos grados de alineación de las células cardíacas encapsuladas en hidrogel circundantes.

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