ECM Degradation and Macrophage Polarization in Endogenous Stem Cell Recruitment
ECM Degradation and Macrophage Polarization in Endogenous Stem Cell Recruitment
批准号:
7912172
负责人:
Vineet Agrawal
金额:
$4.64万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-06 至 2014-07-05
关键词:
AdultCicatrixComplexExtracellular MatrixExtracellular Matrix DegradationFamily suidaeFoundationsFutureGoalsHumanImmune systemIn VitroInflammation ProcessInflammatoryInjuryInvestigationMammalsMediatingNatural regenerationPatientsPeptidesPlayProcessPublic HealthRecovery of FunctionRecruitment ActivityRelative (related person)RoleSiteStem cellsTissuesimplantationin vivomacrophagepublic health relevancerepairedresponse to injuryscaffoldsoft tissuetissue regenerationwound
中文摘要
描述(由申请人提供):损伤后的再生仅限于成年哺乳动物的选定组织。大多数其他组织对损伤的默认反应涉及炎症和瘢痕组织形成的过程(即,修复)。伤口的微环境在成年哺乳动物中决定再生与瘢痕的关系中起着重要作用。在能够再生复杂组织的物种中,招募到伤口微环境中的干细胞促进了一种称为表型再生的过程。由猪源性细胞外基质(ECM)组成的生物支架已成功用于超过一百万例人类患者,以创建伤口微环境,促进各种软组织的位点特异性非炎症修复。在组织损伤后植入ECM支架导致快速降解、生物活性肽的释放、局部巨噬细胞极化和内源性干细胞募集。ECM介导的干细胞体内募集的机制尚不清楚,但可能部分由ECM降解后释放的分子介导。极化的巨噬细胞也能够在体外募集干细胞,但它们对体内内源性干细胞募集的贡献还不清楚。本研究的总体目标是研究:(1)ECM降解在体外和体内干细胞募集中的作用,(2)ECM降解在体外和体内巨噬细胞极化中的作用,以及(3)ECM降解和极化巨噬细胞在体内内源性干细胞募集中的相对贡献。本研究的结果进一步为我们提供了先天免疫系统在促进组织再生中的作用,并将为进一步研究细胞外基质成分,先天免疫系统和内源性干细胞之间相互作用的机制奠定基础。
公共卫生相关性:我们的研究与公共卫生的关系:这些研究的结果将进一步加深我们对先天免疫系统和ECM支架降解在促进功能性组织再生中各自贡献的理解。它将作为未来研究途径的基础,旨在开发更有针对性的治疗方法,以促进人类损伤后的组织再生和功能恢复。
英文摘要
DESCRIPTION (provided by applicant): Regeneration in response to injury is limited to select tissues in adult mammals. The default response to injury in most other tissues involves the processes of inflammation and scar tissue formation (i.e., repair). The microenvironment of the wound plays an important role in determining regeneration versus scar in adult mammals. In species capable of regenerating complex tissues, stem cells recruited to the wound microenvironment promote a process known as epimorphic regeneration. Biologic scaffolds composed of porcine derived extracellular matrix (ECM) have successfully been used in over one million human patients to create a wound microenvironment that promotes site-specific, non-inflammatory repair of a variety of soft tissues. Implantation of an ECM scaffold following tissue injury results in rapid degradation, release of bioactive peptides, local macrophage polarization, and endogenous stem cell recruitment. The mechanisms underlying ECM mediated stem cell recruitment in vivo are well not understood, but may partially be mediated by molecules released following ECM degradation. Polarized macrophages are also capable of recruiting stem cells in vitro, but their contribution to endogenous stem cell recruitment in vivo is not well understood. The overall goal of the present study is to investigate: (1) role of ECM degradation in stem cell recruitment in vitro and in vivo, (2) the role of ECM degradation on macrophage polarization in vitro and in vivo, and (3) the relative contributions of ECM degradation and polarized macrophages upon endogenous stem cell recruitment in vivo. The findings of the present study further inform us on the on the role of the innate immune system in promoting tissue regeneration, and it will serve as the foundation of future studies to further investigate the mechanisms underlying interaction between extracellular matrix components, the innate immune system, and endogenous stem cells.
PUBLIC HEALTH RELEVANCE: THE RELATION OF OUR STUDIES TO PUBLIC HEALTH: The findings from these studies will further our understanding of the respective contributions of the innate immune system and ECM scaffold degradation in promoting functional tissue regeneration. It will serve as the foundation of future avenues of investigation that will aim to develop more targeted therapies for promoting tissue regeneration and functional recovery following injury in humans.
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