Engineering Innervated Muscle-Tendon Constructs for Tissue Regeneration

工程神经支配的肌肉肌腱结构用于组织再生

基本信息

批准号：
8046434
负责人：
LISA M LARKIN
金额：
$ 29.5万
依托单位：
UNIVERSITY OF MICHIGAN AT ANN ARBOR
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-04-11 至 2012-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8046434
关键词：
3-Dimensional Acetylcholine Address Adult Advanced Development Animals Biochemical Biology Bioreactors Caliber Cardiovascular system Cell membrane Characteristics Coculture Techniques Collagen Complex Development Electric Stimulation Engineering Environment Fiber Glycolates Growth Hindlimb Implant In Vitro Infiltration Injury Isometric Exercise Lead Length Limb structure Longitudinal Studies Mechanics Medicine Methodology Muscle Muscle Cells Muscle Contraction Muscle Fibers Musculoskeletal Myosin Heavy Chains Neonatal Nerve Nerve Growth Factors Nerve Tissue Neuromuscular Junction Neurons Phenotype Physical environment Plasmids Polymers Production Protein Isoforms Proteins Rattus Recruitment Activity Silicones Simulate Skeletal Muscle Spinal Cord Stress Structure Study models System Tail Tendon structure Testing Time Tissue Engineering Tissues Transfection Work alpha Bungarotoxin base design end-stage organ failure fetal functional restoration implantation in vitro activity in vivo migration muscle engineering muscle pharmacology nerve supply neurotrophic factor relating to nervous system response sciatic nerve tissue regeneration

项目摘要

DESCRIPTION (provided by applicant): End-stage organ failure or tissue loss is one of the most devastating and costly problems in medicine. The creation of engineered musculoskeletal tissue with functional myotendinous (MTJ) and neuromuscular (NMJ) junctions will not only restore the function of complex tissues such as muscle, tendon, and nerve following traumatic injury, but can also be used as a model for studying developmental muscle biology and muscle pharmacology. We have demonstrated that the co-culture of fetal nerve tissue with fetal or engineered tendon and engineered muscle tissue produces constructs with viable muscle-tendon interfaces that remain intact during force production, and viable neuromuscular junctions that advance the phenotype of the muscle tissue within the construct [1, 2]. The tissues formed express neonatal structures and do not substantially advance functionally or phenotypically in the absence of electrical or mechanical loading. The purpose of this study is to design, fabricate, and evaluate the structural and contractile characteristics of three-dimensional (3-D) engineered tissues containing myotendinous junctions (MTJ) and neuromuscular junctions (NMJ), two of the principal tissue interfaces required for a functional musculoskeletal construct. We propose to study the long-term viability of these constructs; to increase the expression of neurotrophic proteins like glial derived neurotrophic factor (GDNF) and introduce synthetic, engineered, and tissue based conduits to enhance innervation of the muscle constructs; to use bioreactors to place the nerve-tendon- muscle constructs into physical environments which simulate the stress, strain, and contractile activity resembling the mechanical milieu found in hind limb muscles in vivo; and to implant the constructs in vivo to surround the construct with the actual mechanical and biochemical environment of a hindlimb. Our working hypothesis is that an increase in the number of NMJs in conjunction with applied electrical activity in vitro will lead to a more advanced phenotype in the muscle and tendon, increased force production in the engineered muscles, and stronger and more developed tissue interfaces. In vivo implantation of in vitro engineered constructs will further advance the phenotype and functionality of all tissues and tissue interfaces. This project will address the following specific aims: Specific Aim 1. To design and fabricate nerve-tendon-muscle constructs with functional MTJs and NMJs and evaluate both the structural and functional integrity of the constructs at three time points of development. Specific Aim 2. To develop a conduit system to direct the growth of multiple neural extensions towards the muscle construct thus increasing the innervation ratio of the construct. Specific Aim 3. To evaluate the effect of muscle contraction in response to electrical stimulation on the structure and function of the nerve-tendon-muscle construct. Specific Aim 4. To evaluate the effect of an in vivo implantation into a host animal on the structure and function of the nerve-muscle tendon construct at four weeks.

描述（由申请人提供）：终末期器官衰竭或组织损失是医学上最具破坏性和成本最高的问题之一。具有功能性肌腱（MTJ）和神经肌肉（NMJ）连接的工程化肌肉骨骼组织的创建不仅可以恢复外伤后肌肉、肌腱和神经等复杂组织的功能，还可以用作研究发育的模型肌肉生物学和肌肉药理学。我们已经证明，胎儿神经组织与胎儿或工程肌腱和工程肌肉组织的共培养产生的结构具有在力产生过程中保持完整的可行的肌肉肌腱界面，以及可促进胎儿内肌肉组织表型的可行的神经肌肉接头。构建 [1, 2]。形成的组织表达新生儿结构，并且在没有电或机械负荷的情况下不会在功能或表型上显着进步。本研究的目的是设计、制造和评估包含肌腱接头 (MTJ) 和神经肌肉接头 (NMJ) 的三维 (3-D) 工程组织的结构和收缩特性，这两种主要组织界面是功能性肌肉骨骼结构。我们建议研究这些结构的长期可行性；增加神经营养蛋白如神经胶质源性神经营养因子（GDNF）的表达，并引入合成的、工程化的和基于组织的管道来增强肌肉结构的神经支配；使用生物反应器将神经-肌腱-肌肉结构放入物理环境中，模拟压力、应变和收缩活动，类似于体内后肢肌肉中发现的机械环境；并将构建体植入体内，以用后肢的实际机械和生化环境包围该构建体。我们的工作假设是，NMJ 数量的增加与体外施加的电活动相结合将导致肌肉和肌腱的更先进的表型，工程肌肉中产生的力量增加，以及更强大和更发达的组织界面。体外工程构建体的体内植入将进一步改善所有组织和组织界面的表型和功能。该项目将实现以下具体目标：具体目标 1. 设计和制造具有功能性 MTJ 和 NMJ 的神经-肌腱-肌肉结构，并在三个开发时间点评估该结构的结构和功能完整性。具体目标 2. 开发一种导管系统，引导多个神经延伸向肌肉结构生长，从而增加该结构的神经支配比率。具体目标 3. 评估电刺激引起的肌肉收缩对神经-肌腱-肌肉结构的结构和功能的影响。具体目标 4. 评估体内植入宿主动物 4 周后对神经肌肉腱结构的结构和功能的影响。

项目成果

期刊论文数量（6）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Growth Factors for Skeletal Muscle Tissue Engineering.

DOI：
10.1159/000444671
发表时间：
2016
期刊：
Cells, tissues, organs
影响因子：
0
作者：
Syverud BC;VanDusen KW;Larkin LM
通讯作者：
Larkin LM

Development of a scaffoldless three-dimensional engineered nerve using a nerve-fibroblast co-culture.

DOI：
10.1007/s11626-009-9260-z
发表时间：
2010-05
期刊：
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
影响因子：
2.1
作者：
Baltich, Jennifer;Hatch-Vallier, Leah;Adams, Aaron M.;Arruda, Ellen M.;Larkin, Lisa M.
通讯作者：
Larkin, Lisa M.

TGF-β1 enhances contractility in engineered skeletal muscle.

DOI：
10.1002/term.551
发表时间：
2013-07
期刊：
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE
影响因子：
3.3
作者：
Weist, Michael R.;Wellington, Michael S.;Bermudez, Jacob E.;Kostrominova, Tatiana Y.;Mendias, Christopher L.;Arruda, Ellen M.;Larkin, Lisa M.
通讯作者：
Larkin, Lisa M.

Use of adipose-derived stem cells to fabricate scaffoldless tissue-engineered neural conduits in vitro.