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HYPOTHERMIC AND CRYOPRESERVATION OF HUMAN BLOOD VESSELS

HYPOTHERMIC AND CRYOPRESERVATION OF HUMAN BLOOD VESSELS
人体血管的低温和冷冻保存
批准号:
6140066
负责人:
Robert G Van Buskirk
金额:
$9.58万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-06-01 至 2002-05-31

项目摘要

项目成果

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中文摘要
翻译
BioLife Technologies (BLT)成立于1998年3月31日。BLT的主要任务是开发改进的低温和低温保存解决方案,旨在维持细胞,组织和器官处于接近假死状态。心脏截瘫、器官移植和一些不受管制的市场已成为发展目标。该I期SBIR计划使用四种心血管细胞株作为体外工具,以帮助开发针对人类血管保存进行优化的未来HTS解决方案。BLT的低温溶液,HypoThermosol(R) (HTS)系列,在保护肾脏、心脏和皮肤细胞方面比杜邦-默克公司十年前生产的ViaSpan(R)更好。ViaSpan(R)目前在保存液业务中占有最大的市场份额,但ViaSpan(R)的设计并非基于现代分子生物学研究。BLT已经启动了一项积极的计划,以确定在长时间低温和低温保存期间细胞死亡的分子基础,以便了解这些事件可以导致新一代的低温解决方案。由于BLT的早期成功,HTS目前正用于胰岛移植I期临床试验。本研究提出的DNA凝胶表明,低温保存时间过长或低温保存的细胞在返回常温(37℃)两天后会因细胞凋亡(程序性细胞死亡)而死亡。添加凋亡抑制剂的HTS可阻断这一过程,提高HTS的性能。BLT目前有一项专利正在申请中,该专利将允许BLT独家设计未来的HTS解决方案,从而抑制细胞凋亡。这个第一阶段项目的具体目标是:(a)确定保存诱导的血管细胞损伤导致的细胞凋亡和坏死的相对贡献;(b)确定哪种细胞凋亡抑制剂在提高HTS疗效方面最有效;(c)确定坏死/凋亡、线粒体细胞色素c渗漏和线粒体跨膜电位丧失之间的关系(如果有的话);(d)确定延长保存是否会缩短端粒,从而导致细胞过早衰老。II期研究将致力于HTS保存完整的人类血管,这项工作将与我们的合作伙伴crylife公司共同完成。拟议的商业应用:BioLife正在开发新一代的保存解决方案,将改善用于临床心血管应用的人类血管的长期储存。这些解决方案还将有助于保存目前正在开发的未来组织工程血管。
英文摘要
BioLife Technologies (BLT) was incorporated on March 31, 1998. BLT's primary mission is to develop improved hypothermic and cryopreservation solutions designed to maintain cells, tissues and organs in a near state of suspended animation. Cardioplegia, organ transplant and selected non- regulated markets have been targeted for development. This Phase I SBIR proposes to use four cardiovascular cell strains as in vitro tools to help develop a future HTS solution that is optimized for human blood vessel preservation. BLT's hypothermic solutions, the HypoThermosol(R) (HTS) series, are better at cold-protecting kidney, heart and skin cells than is ViaSpan(R) - a product produced by DuPont-Merck ten years ago. ViaSpan(R) currently commands the largest market share in the preservation solution business, but the design of ViaSpan(R) is not based on modern molecular biology investigations. BLT has launched an aggressive program to determine the molecular basis of cell death during extended hypothermic and cryopreservation storage so that knowledge of these events can lead to a new generation of hypothermic solutions. As a result of BLT's early success, HTS is currently being used in a pancreatic islet transplantation Phase I clinical trial. DNA gels presented in this proposal demonstrate that cells cold stored for too long or cryopreserved die by apoptosis (programmed cell death) two days after they are returned to normothermic (37 degrees C) temperatures. HTS supplemented with apoptosis inhibitors blocks this process and improves HTS's performance. BLT currently has a patent pending that will allow BLT the exclusive right to formulate future HTS solutions by design so that apoptosis is inhibited. The Specific Aims of this Phase I project are to (a) determine the relative contributions of apoptosis and necrosis as a consequence of preservation-induced cellular injury to blood vessel cells; (b) determine which apoptosis inhibitors are the most effective at increasing HTS efficacy; (c) determine the relationship, if any, between necrosis/apoptosis, cytochrome C leakage from mitochondria, and loss of mitochondrial transmembrane potential; and (d) determine if extended preservation shortens telomeres and as a consequence precipitates premature cell senescence. Phase II studies will be devoted to HTS preservation of intact human blood vessels - work to be accomplished with our collaborator, CryoLife Inc. PROPOSED COMMERCIAL APPLICATIONS: BioLife is developing a new generation of preservation solutions that will improve the long term storage of human blood vessels used for clinical cardiovascular applications. The solutions will also facilitate preservation of future, tissue engineered blood vessels currently under development.
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