ID:4005 Injectable Cell Delivery Constructs for Myocardial Tissue Engineering

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Hsing-Wen Sung Chieh-Cheng Huang Ding-Yuan Chen Chun-Wen Hsiao Wen-Yu Lee Yen Chang

Abstract

Cell transplantation via direct intramuscular injection is a promising therapy for patients with ischemic diseases. However, following injections, retention of transplanted cells in engrafted areas remains problematic, and can be deleterious to cell-transplantation therapy. In this presentation, a thermo-responsive hydrogel system composed of aqueous methylcellulose (MC) blended with phosphate-buffered saline is constructed to grow cell sheet fragments and cell bodies for the treatment of ischemic diseases. The as-prepared MC hydrogel system undergoes a sol–gel reversible transition upon heating or cooling at approximately 32 °C. Via this unique property, the grown cell sheet fragments (cell bodies) can be harvested without using proteolytic enzymes; consequently, their inherent extracellular matrices (ECMs) and integrative adhesive agents remain well preserved. In animal studies using rats and pigs with experimentally created myocardial infarction, the injected cell sheet fragments (cell bodies) become entrapped in the interstices of muscular tissues and adhere to engraftment sites, while a minimal number of cells exist in the group receiving dissociated cells. Moreover, transplantation of cell sheet fragments (cell bodies) significantly increases vascular density, thereby improving the function of an infarcted heart.

These experimental results demonstrate that cell sheet fragments (cell bodies) function as a cell-delivery construct by providing a favorable ECM environment to retain transplanted cells locally and consequently, improving the efficacy of therapeutic cell transplantation

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How to Cite
SUNG, Hsing-Wen et al. ID:4005 Injectable Cell Delivery Constructs for Myocardial Tissue Engineering. Biomedical Research and Therapy, [S.l.], v. 4, n. S, p. S7, sep. 2017. ISSN 2198-4093. Available at: <http://www.bmrat.org/index.php/BMRAT/article/view/215>. Date accessed: 23 oct. 2017. doi: https://doi.org/10.15419/bmrat.v4iS.215.
Section
Oral Abstracts