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在啮齿动物部分后肢模型中实现血管化复合异体移植物的零上非冻结。

Sub-zero non-freezing of vascularized composite allografts in a rodent partial hindlimb model.

机构信息

Center for Engineering for Medicine and Surgery, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Shriners Children's Boston, Boston, MA, USA; Department of Plastic, Reconstructive and Hand Surgery, University Medical Center Utrecht, Utrecht, the Netherlands; Vascularized Composite Allotransplantation Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Shriners Children's Boston, Boston, MA, USA; Vascularized Composite Allotransplantation Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Department of Plastic, Reconstructive et Aesthetic Surgery, Hôpital Paris Saint-Joseph, Paris, France.

出版信息

Cryobiology. 2024 Sep;116:104950. doi: 10.1016/j.cryobiol.2024.104950. Epub 2024 Aug 24.

DOI:10.1016/j.cryobiol.2024.104950
PMID:39134131
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11404353/
Abstract

Ischemia is a major limiting factor in Vascularized Composite Allotransplantation (VCA) as irreversible muscular injury can occur after as early as 4-6 h of static cold storage (SCS). Organ preservation technologies have led to the development of storage protocols extending rat liver ex vivo preservation up to 4 days. Development of such a protocol for VCAs has the added challenge of inherent ice nucleating factors of the graft, therefore, this study focused on developing a robust protocol for VCA supercooling. Rodent partial hindlimbs underwent subnormothermic machine perfusion (SNMP) with several loading solutions, followed by a storage solution with cryoprotective agents (CPA) developed for VCAs. Storage occurred in suspended animation for 24h and VCAs were recovered using SNMP with modified Steen. This study shows a robust VCA supercooling preservation protocol in a rodent model. Further optimization is expected to allow for its application in a transplantation model, which would be a breakthrough in the field of VCA preservation.

摘要

缺血是血管化复合组织同种异体移植(VCA)的主要限制因素,因为在静态冷储存(SCS)后仅 4-6 小时就可能发生不可逆的肌肉损伤。器官保存技术已经导致储存方案的发展,将大鼠肝脏离体保存时间延长至 4 天。开发这样一种 VCAs 的方案具有移植物固有的成冰因子的额外挑战,因此,本研究集中于开发一种强大的 VCA 过冷方案。啮齿动物部分后肢进行亚体温机器灌注(SNMP),并用几种加载溶液,然后用开发用于 VCAs 的含冷冻保护剂(CPA)的储存溶液。储存 24 小时,使用改良的 Steen 进行 SNMP 恢复 VCAs。本研究在啮齿动物模型中展示了一种强大的 VCA 过冷保存方案。进一步的优化有望使其在移植模型中得到应用,这将是 VCA 保存领域的一个突破。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/6f47ee8ca23a/nihms-2020795-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/cc64f5a50fbe/nihms-2020795-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/b5bd39b28406/nihms-2020795-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/9cd7e04aa3f7/nihms-2020795-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/e15b4ed9b26f/nihms-2020795-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/b038ac842a62/nihms-2020795-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/6f47ee8ca23a/nihms-2020795-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/cc64f5a50fbe/nihms-2020795-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/b5bd39b28406/nihms-2020795-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/9cd7e04aa3f7/nihms-2020795-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/e15b4ed9b26f/nihms-2020795-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/b038ac842a62/nihms-2020795-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b7/11404353/6f47ee8ca23a/nihms-2020795-f0006.jpg

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本文引用的文献

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