Title of article :
Granulocyte-based immune response against decellularized or glutaraldehyde cross-linked vascular tissue
Author/Authors :
Erwin Rieder، نويسنده , , Anneliese Nigisch، نويسنده , , Barbara Dekan، نويسنده , , Marie-Theres Kasimir، نويسنده , , Ferdinand Mühlbacher، نويسنده , , Ernst Wolner، نويسنده , , Paul Simon، نويسنده , , Günter Weigel، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
9
From page :
5634
To page :
5642
Abstract :
Supporting structures derived from biological tissue have been used in numerous tissue-engineering applications. This study focuses on the immune response of human leukocytes toward decellularized or glutaraldehyde (GA) cross-linked vascular tissue in vitro. Porcine and human pulmonary roots were sterilized with antibiotics, decellularized or cross-linked with GA. Proteins of the vascular tissue were extracted and the migratory response of human leukocytes toward protein extracts was examined using an in vitro migration chamber. Transmigrated leukocytes were counted and subsets (lymphocytes, monocytes, granulocytes) analyzed by flow cytometry. Decellularization significantly reduced the migration of monocytes compared to native porcine tissue. Although the proportion of transmigrating lymphocytes was much lower, decellularization again reduced the migratory response. Surprisingly, after decellularization granulocyte migration was still significantly higher than the negative control. Results comparable to those obtained with porcine material were found when human tissue was used for the experiments. Interestingly, migratory behavior toward extracts of GA-fixed porcine tissue was similar to that of decellularized specimens. We have shown that decellularization of vascular tissue reduces lymphocyte and monocyte recruitment comparable to cross-linking treatment. However, the migration of granulocytes, which are also known to be strongly involved in early inflammatory reactions, could be abolished neither by decellularization nor by fixation with GA.
Keywords :
Tissue engineering , immune response , ECM , leukocytes
Journal title :
Biomaterials
Serial Year :
2006
Journal title :
Biomaterials
Record number :
547226
Link To Document :
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