15.08.2018 Views

Abstracts Book - IMRC 2018

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

• SB3-O009<br />

SCAFFOLD FOR TISSUE ENGINEERING FROM EXTRACELLULAR<br />

MATRIX OF MYOCARDIUM<br />

Abraham Israel Muñoz Ruiz 1 , Hector Flores 1 , Amaury Pozos Guillen 1 , Diana M. Escobar García 1<br />

1 Universidad Autónoma de San Luis Potosí, Laboratorio De Ciencias Básicas, Mexico.<br />

Introduction. Heart transplantation remains as the definitive treatment for the<br />

majority of advanced cardiac diseases, however the quantity of donated organs is<br />

limited and the patient require specific conditions for the procedure to be carried<br />

out.Tissue engineering (TE) is a field of medicine that applies principles of the<br />

biological sciences and engineering for the design of tissue substitutes. The main<br />

components of TE are: cells, biomaterials and the combined use of both.<br />

Biomaterials are used to design threedimensional scaffolds that provide a site to<br />

cells for adhesion, proliferation and differentiation. The topography, chemical<br />

composition, microstructure and mechanical properties have a relevant influence<br />

on cellular behavior. In a living organism cells are surrounded by an extracellular<br />

matrix, so it is logical to consider that can act as an ideal scaffold. The objective of<br />

this work is to obtain a scaffold of a decellularized cardiac organ for tissue<br />

engineering.<br />

Methodology. Obtaining Heart. Three male Wistar rats were sacrificed. The rib cage<br />

was subjected to a dissection and the heart was subsequently removed. The heart<br />

was perfused with a pediatric feeding tube with sterile PBS 1X. Decellularization.<br />

The decellularization process was carried out using different solutions (Trypsin, PBS<br />

+ SFB, Triton + ammonium hydroxide, SDS). Extraction of DNA. Cardiac tissue was<br />

mechanically crushed to obtain a representative sample of DNA. A kit of DNA<br />

extraction was used to make a quantification with a NanoDrop equipment. PCR<br />

amplification - GAPDH gene. For amplification was used a comercial kit (Master Mix<br />

+ Primer F + Primer R + Ultrapure water + 250 ng of DNA. The sample was placed<br />

on an agarose gel and read in a photodocumentator.<br />

Results. DNA extraction showed a quantification of 12.4 ng/μl. The PCR<br />

amplification showed that the GAPDH gene was not present.<br />

Conclusion. The low amount of DNA and low expression of GAPDH mean that the<br />

decellularization process was successful. The extracellular matrix of myocardium<br />

could act as a scaffold for tissue engineering.<br />

Keywords: Scaffold, Decellularization, Myocardium<br />

Presenting authors email: a.israel.mr@gmail.com

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!