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Develop a combinatorial therapy for spinal cord injury

开发脊髓损伤的组合疗法

基本信息

批准号：
10408725
负责人：
SHUXIN LI
金额：
$ 34.29万
依托单位：
TEMPLE UNIV OF THE COMMONWEALTH
依托单位国家：
美国
项目类别：
财政年份：
2018
资助国家：
美国
起止时间：
2018-06-01 至 2024-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10408725
关键词：
Adult Afferent Neurons Antibodies Axon CD45 Antigens Chest Chondroitin Sulfate Proteoglycan Cicatrix Combined Modality Therapy Corticospinal Tracts Development Dorsal Environment Failure Family Fiber Genetic Goals Growth Individual Injury Knock-out Knockout Mice LAR tyrosine phosphatase receptor Lesion Locomotion Locomotor Recovery Mammals Mediating Modeling Molecular Target Movement Mus Natural regeneration Nerve Regeneration Neuronal Plasticity Neurons Peptides Pharmacology Phosphoric Monoester Hydrolases Pilot Projects Play Population Projection Positioning Attribute Protein Tyrosine Phosphatase Rattus Receptor Signaling Recovery Recovery of Function Rodent Role Sensory Signal Pathway Signal Transduction Site Spinal Cord Contusions Spinal cord injury The Jackson Laboratory Therapeutic Transgenic Organisms Treatment Effectiveness WNT Signaling Pathway antagonist axon growth axon guidance axon injury axon regeneration base central nervous system injury combinatorial compare effectiveness design effectiveness evaluation extracellular in vivo inhibitor injured injury and repair neuronal growth novel strategies optimal treatments receptor repair strategy sigma receptors synaptogenesis synergism treatment optimization

项目摘要

Project Summary Severed CNS axons fail to regenerate largely because of the reduced intrinsic growth capacity of adult neurons and poor environment for axon extension. The Co-I's Lab finds that the Wnt family molecules and their receptors are upregulated after spinal cord injury (SCI) and mediates regrowth Among adult failure of injured fiber tracts. several Wnt receptors, Ryk is crucial for mediating repulsive axon growth during development and in CNS after injury.Chondroitin sulfate proteoglycans (CSPGs) generated by glial scars strongly suppress axon extension and are major extrinsic molecular targets for treating CNS injury. The PI's group designed small peptides to block functions of CSPG receptors LAR and PTPσ by targeting their critical activity domains and demonstrated their high efficiency for promoting axon growth. Blocking each of the two receptors with 3 combined peptides promotes robust regeneration of injured CNS axons. We hypothesize that inhibiting both Wnt and CSPG signals represents a dual approach of enhancing neuronal growth capacity and reducing environmental inhibitory influence at the lesion site. We propose to stimulate robust axon regrowth in adult rodents with transection or contusion SCI by inhibiting Ryk and LAR/PTPσ with genetic and pharmacological approaches available in our labs. In Aim 1, we will study synergistic actions of transgenically deleting Ryk plus each of LAR/PTPσ receptors on promoting axon regeneration and recovery in mice with SCI. We will determine whether deleting Ryk plus LAR or Ryk plus PTPσ receptors acts synergistically to stimulate axon growth and enhance neuronal plasticity in double knockout mice after SCI. In Aim 2, we will determine whether blocking each of Ryk, LAR and PTPσ receptors with antibody or selective antagonists pharmacologically promotes axon regeneration and recovery in adult rats with SCI. We will compare effectiveness of the treatments that target individual receptors in promoting regrowth of multiple descending tracts and recovery of locomotor functions after SCI. In Aim 3, we will study whether combination therapies that block two or three receptors yield better axon regrowth and functional recovery in rats with transection or contusion SCI, aiming to identify the optimal therapy for mammals with SCI. Based on the promising results from our pilot studies, we predict that our combined strategies will promote dramatic regeneration of injured axon tracts and recovery of locomotion function in vivo. Our novel strategy of administering deliverable compounds post-injury may facilitate development of a practical combinatorial therapy for CNS lesions.

项目总结

项目成果

期刊论文数量（13）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Liver Kinase B1 Functions as a Regulator for Neural Development and a Therapeutic Target for Neural Repair.

DOI：
10.3390/cells11182861
发表时间：
2022-09-14
期刊：
Cells
影响因子：
6
作者：
通讯作者：

The Atr-Chek1 pathway inhibits axon regeneration in response to Piezo-dependent mechanosensation.

ATR-CHEK1途径响应压电依赖性机械敏，抑制轴突再生。

DOI：
10.1038/s41467-021-24131-7
发表时间：
2021-06-22
期刊：
Nature communications
影响因子：
16.6
作者：
Li F;Lo TY;Miles L;Wang Q;Noristani HN;Li D;Niu J;Trombley S;Goldshteyn JI;Wang C;Wang S;Qiu J;Pogoda K;Mandal K;Brewster M;Rompolas P;He Y;Janmey PA;Thomas GM;Li S;Song Y
通讯作者：
Song Y

Glial Metabolic Rewiring Promotes Axon Regeneration and Functional Recovery in the Central Nervous System.

DOI：
10.1016/j.cmet.2020.08.015
发表时间：
2020-11-03
期刊：
Cell metabolism
影响因子：
29
作者：
Li F;Sami A;Noristani HN;Slattery K;Qiu J;Groves T;Wang S;Veerasammy K;Chen YX;Morales J;Haynes P;Sehgal A;He Y;Li S;Song Y
通讯作者：
Song Y

Respiratory axon regeneration in the chronically injured spinal cord.

长期受伤的脊髓中的呼吸轴突再生。

DOI：
10.1016/j.nbd.2021.105389
发表时间：
2021-07
期刊：
Neurobiology of disease
影响因子：
6.1
作者：
Cheng L;Sami A;Ghosh B;Goudsward HJ;Smith GM;Wright MC;Li S;Lepore AC
通讯作者：
Lepore AC

LAR inhibitory peptide promotes recovery of diaphragm function and multiple forms of respiratory neural circuit plasticity after cervical spinal cord injury.

DOI：
10.1016/j.nbd.2020.105153
发表时间：
2021-01
期刊：
Neurobiology of disease
影响因子：
6.1
作者：
Cheng L;Sami A;Ghosh B;Urban MW;Heinsinger NM;Liang SS;Smith GM;Wright MC;Li S;Lepore AC
通讯作者：
Lepore AC