Diabetic skin influences on outgrowth of human iPSC-derived sensory axons
糖尿病皮肤影响人类 iPSC 衍生的感觉轴突的生长
基本信息
- 批准号:10539034
- 负责人:
- 金额:$ 45.03万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-07-01 至 2024-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAffectAfferent NeuronsAxonBackBiopsyCell LineCellsCharacteristicsClinicalClinical ProtocolsCoculture TechniquesCutaneousDermisDevelopmentDiabetes MellitusDiabetic NeuropathiesDistalEnvironmentEpidermisFiberFibroblastsFutureGrowthHumanImpairmentIn VitroIntrinsic factorKnowledgeMicrofluidic MicrochipsMicrofluidicsModelingNatural regenerationNerveNerve DegenerationNerve FibersNeural ConductionNeuronsNeuropathyPatientsPeripheral Nervous System DiseasesPersonsPhysiologyPlayPositioning AttributeResearchRoleSensorySeveritiesSkinSkin TissueSystemTissuesadverse outcomeaxon growthaxon regenerationaxonal degenerationaxonal sproutingbiological systemsblood glucose regulationdensitydiabeticdiabetic patientdiagnostic toolexperimental studyhealth differencein vivoinduced pluripotent stem cellneuronal cell bodynew therapeutic targetnovelregenerativerepairedtherapeutic targettreatment strategy
项目摘要
Project Summary:
This proposal details a new research plan to examine the differential effects of neuronal origin
and axonal target environment on nerves from people with diabetes mellitus 2 (DM2) to
understand why these nerves degenerate and have reduced plasticity compared to their heathy
counterparts, especially within the epidermis. Axon growth of sensory neurons derived from
human induced pluripotent stem cells (iPSCs) will be studied in the presence of skin biopsied
from control subjects and patients with diabetes and varying degrees of peripheral neuropathy.
We hypothesize:
1) That cellular origin matters and that sensory axons derived from iPSCs of
subjects with DM2 and peripheral neuropathy will grow and regenerate more
slowly than sensory neurons derived from healthy control iPSCs.
2) That the regenerative environment also plays an important role, perhaps more
important than neuronal origin: that sensory axons, irrespective of their origin,
will regenerate more slowly on a matrix of skin from subjects with DM2 and
peripheral neuropathy compared to a matrix of skin from healthy control
subjects.
Understanding the role of these different potential influences on human axonal
regeneration will place us in a better position in the future to identify the molecules involved and
therapeutic targets for diabetic neuropathy- a condition that has defied meaningful clinical
advances beyond optimizing glucose control.
Sensory neurons derived from human iPSCs hold promise for advancing the field of
small fiber neuropathy in general, including diabetic peripheral neuropathy (DPN). However,
interactions of iPSC-derived sensory neurons with the epidermis have not been explored.
Therefore, it is important to perform novel experiments, such as those proposed here, that
specifically examine axons of iPSC-derived sensory neurons to determine potential factors that
influence their degeneration when they are in milieu, over biopsied skin that mimics human
conditions.
We are addressing this knowledge gap by utilizing microfluidic chambers that separate
axons from neuronal cell bodies in order to study the basic pathobiology of the distal sensory
axons of diabetic patients. Through this proposal, we anticipate the development of a system
derived from human cells to interrogate factors that inhibit axonal plasticity in DPN.
项目概要:
该提案详细介绍了一项新的研究计划,以检查神经元起源的差异效应
2 型糖尿病 (DM2) 患者的神经和轴突目标环境
了解为什么这些神经与健康神经相比会退化并降低可塑性
对应物,尤其是在表皮内。感觉神经元的轴突生长源自
人类诱导多能干细胞 (iPSC) 将在皮肤活检的情况下进行研究
来自对照受试者和患有糖尿病和不同程度周围神经病变的患者。
我们假设:
1) 细胞起源很重要,感觉轴突源自 iPSC
患有 DM2 和周围神经病变的受试者将生长和再生更多
比来自健康对照 iPSC 的感觉神经元慢。
2)再生环境也发挥着重要作用,也许更重要
比神经元起源更重要的是:感觉轴突,无论其起源如何,
DM2 患者的皮肤基质上的再生速度会更慢,并且
与健康对照的皮肤基质相比,周围神经病变
科目。
了解这些不同的潜在影响对人类轴突的作用
再生将使我们在未来能够更好地识别所涉及的分子并
糖尿病神经病变的治疗目标——这种疾病在临床上尚无意义
超越优化血糖控制的进步。
源自人类 iPSC 的感觉神经元有望推动这一领域的发展
一般小纤维神经病,包括糖尿病周围神经病(DPN)。然而,
iPSC 衍生的感觉神经元与表皮的相互作用尚未被探索。
因此,进行新颖的实验非常重要,例如这里提出的实验,
专门检查 iPSC 衍生的感觉神经元的轴突,以确定潜在的因素
当它们处于模仿人类的活检皮肤环境中时,会影响它们的退化
状况。
我们正在通过利用微流体室来解决这一知识差距
来自神经元细胞体的轴突,以研究远端感觉的基本病理学
糖尿病患者的轴突。通过这个提案,我们预计开发一个系统
源自人类细胞,用于询问抑制 DPN 中轴突可塑性的因素。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Mohamed H Farah其他文献
Mohamed H Farah的其他文献
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{{ truncateString('Mohamed H Farah', 18)}}的其他基金
Axonal pathogenesis of human iPSC-derived motor neurons
人 iPSC 来源的运动神经元的轴突发病机制
- 批准号:
10604850 - 财政年份:2022
- 资助金额:
$ 45.03万 - 项目类别:
BACE1 inhibition in injured peripheral nerve and a neuropathy mouse models
BACE1 抑制损伤周围神经和神经病小鼠模型
- 批准号:
8640221 - 财政年份:2012
- 资助金额:
$ 45.03万 - 项目类别:
BACE1 inhibition in injured peripheral nerve and a neuropathy mouse models
BACE1 抑制损伤周围神经和神经病小鼠模型
- 批准号:
8481608 - 财政年份:2012
- 资助金额:
$ 45.03万 - 项目类别:
BACE1 inhibition in injured peripheral nerve and a neuropathy mouse models
BACE1 抑制损伤周围神经和神经病小鼠模型
- 批准号:
8340085 - 财政年份:2012
- 资助金额:
$ 45.03万 - 项目类别:
BACE1 inhibition in injured peripheral nerve and a neuropathy mouse models
BACE1 抑制损伤周围神经和神经病小鼠模型
- 批准号:
9041692 - 财政年份:2012
- 资助金额:
$ 45.03万 - 项目类别:
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