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幼年非人灵长类动物模型中生物支架二尖瓣置换术后的新生瓣膜组织形态学

De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model.

作者信息

Gonzalez Brittany A, Perez Gonzalez Marcos, Scholl Frank, Bibevski Steven, Ladich Elena, Bibevski Jennifer, Morales Pablo, Lopez Jesus, Casares Mike, Brehier Vincent, Hernandez Lazaro, Ramaswamy Sharan

机构信息

Department of Biomedical Engineering, Florida International University, Miami, FL 33174, USA.

Memorial Healthcare System, Joe DiMaggio Children's Hospital, Hollywood, FL 33021, USA.

出版信息

Bioengineering (Basel). 2021 Jul 16;8(7):100. doi: 10.3390/bioengineering8070100.

DOI:10.3390/bioengineering8070100
PMID:34356207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8301182/
Abstract

The utility of implanting a bioscaffold mitral valve consisting of porcine small intestinal submucosa (PSIS) in a juvenile baboon model (12 to 14 months old at the time of implant; = 3) to assess their in vivo tissue remodeling responses was investigated. Our findings demonstrated that the PSIS mitral valve exhibited the robust presence of de novo extracellular matrix (ECM) at all explantation time points (at 3-, 11-, and 20-months). Apart from a significantly lower level of proteoglycans in the implanted valve's annulus region ( < 0.05) at 3 months compared to the 11- and 20-month explants, there were no other significant differences ( > 0.05) found between any of the other principal valve ECM components (collagen and elastin) at the leaflet, annulus, or chordae tendinea locations, across these time points. In particular, neochordae tissue had formed, which seamlessly integrated with the native papillary muscles. However, additional processing will be required to trigger accelerated, uniform and complete valve ECM formation in the recipient. Regardless of the specific processing done to the bioscaffold valve, in this proof-of-concept study, we estimate that a 3-month window following bioscaffold valve replacement is the timeline in which complete regeneration of the valve and integration with the host needs to occur.

摘要

研究了在幼年狒狒模型(植入时12至14个月大;n = 3)中植入由猪小肠黏膜下层(PSIS)组成的生物支架二尖瓣以评估其体内组织重塑反应的效用。我们的研究结果表明,PSIS二尖瓣在所有外植时间点(3个月、11个月和20个月)均表现出大量新生细胞外基质(ECM)的存在。与11个月和20个月的外植体相比,植入瓣膜的瓣环区域在3个月时蛋白聚糖水平显著较低(P<0.05),在这些时间点,小叶、瓣环或腱索位置的任何其他主要瓣膜ECM成分(胶原蛋白和弹性蛋白)之间均未发现其他显著差异(P>0.05)。特别是,新腱索组织已经形成,并与天然乳头肌无缝整合。然而,需要额外的处理来触发受体中瓣膜ECM的加速、均匀和完全形成。无论对生物支架瓣膜进行何种具体处理,在这项概念验证研究中,我们估计生物支架瓣膜置换后的3个月窗口期是瓣膜完全再生并与宿主整合所需的时间线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/ada6af69ddb8/bioengineering-08-00100-g014.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/3d79fb1c02a1/bioengineering-08-00100-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/e67cbdfb1795/bioengineering-08-00100-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/49e552cc1094/bioengineering-08-00100-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/f98db7d15018/bioengineering-08-00100-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/1f61a71dafff/bioengineering-08-00100-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/946e50c9cf69/bioengineering-08-00100-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/d2e4d3fcae14/bioengineering-08-00100-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/ada6af69ddb8/bioengineering-08-00100-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/e4872fe9444a/bioengineering-08-00100-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/4192c92d26c0/bioengineering-08-00100-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/d04bfbeb95cd/bioengineering-08-00100-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/276724c05be8/bioengineering-08-00100-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/efefdeeb805e/bioengineering-08-00100-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/174a8e4b9240/bioengineering-08-00100-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/3d79fb1c02a1/bioengineering-08-00100-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/e67cbdfb1795/bioengineering-08-00100-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/49e552cc1094/bioengineering-08-00100-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/f98db7d15018/bioengineering-08-00100-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/1f61a71dafff/bioengineering-08-00100-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/946e50c9cf69/bioengineering-08-00100-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/d2e4d3fcae14/bioengineering-08-00100-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ce/8301182/ada6af69ddb8/bioengineering-08-00100-g014.jpg

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