scholarly journals The effect of systemic PTEN antagonist peptides on axon growth and functional recovery after spinal cord injury

Biomaterials ◽  
2014 ◽  
Vol 35 (16) ◽  
pp. 4610-4626 ◽  
Author(s):  
Yosuke Ohtake ◽  
Dongsun Park ◽  
P.M. Abdul-Muneer ◽  
Hui Li ◽  
Bin Xu ◽  
...  
2009 ◽  
Vol 26 (7) ◽  
pp. 955-964 ◽  
Author(s):  
Tomohiro Miyashita ◽  
Masao Koda ◽  
Keiko Kitajo ◽  
Masashi Yamazaki ◽  
Kazuhisa Takahashi ◽  
...  

2017 ◽  
Vol 38 (6) ◽  
pp. 1366-1382 ◽  
Author(s):  
Zoe C. Hesp ◽  
Rim Y. Yoseph ◽  
Ryusuke Suzuki ◽  
Peter Jukkola ◽  
Claire Wilson ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Fei Lei ◽  
Wen He ◽  
Xinggui Tian ◽  
Qingzhong Zhou ◽  
Lipeng Zheng ◽  
...  

The reparative process following spinal cord injury (SCI) is extremely complicated. Cells in the microenvironment express multiple inhibitory factors that affect axonal regeneration over a prolonged period of time. The axon growth inhibitory factor glycogen synthase kinase-3 (GSK-3) is an important factor during these processes. TDZD-8 (4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione) is the most effective and specific non-ATP-competitive inhibitor of GSK-3. Here, we show that administering TDZD-8 after SCI was associated with significantly inhibited neuronal apoptosis, upregulated GAP-43 expression, increased density of cortical spinal tract fibers around areas of injury, and increased Basso, Beattie, and Bresnahan (BBB) scores in the lower limbs. These findings support the notion that GSK-3 inhibitors promote neuronal cell regeneration and lower limb functional recovery.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Dayu Pan ◽  
Fuhan Yang ◽  
Shibo Zhu ◽  
Yongjin Li ◽  
Guangzhi Ning ◽  
...  

AbstractSpinal cord injury (SCI) can lead to severe loss of motor and sensory function with high disability and mortality. The effective treatment of SCI remains unknown. Here we find systemic injection of TGF-β neutralizing antibody induces the protection of axon growth, survival of neurons, and functional recovery, whereas erythropoietin-producing hepatoma interactor B2 (EphrinB2) expression and fibroblasts distribution are attenuated. Knockout of TGF-β type II receptor in fibroblasts can also decrease EphrinB2 expression and improve spinal cord injury recovery. Moreover, miR-488 was confirmed to be the most upregulated gene related to EphrinB2 releasing in fibroblasts after SCI and miR-488 initiates EphrinB2 expression and physical barrier building through MAPK signaling after SCI. Our study points toward elevated levels of active TGF-β as inducer and promoters of fibroblasts distribution, fibrotic scar formation, and EphrinB2 expression, and deletion of global TGF-β or the receptor of TGF-β in Col1α2 lineage fibroblasts significantly improve functional recovery after SCI, which suggest that TGF-β might be a therapeutic target in SCI.


2020 ◽  
Vol 11 ◽  
Author(s):  
Roxana Rodríguez-Barrera ◽  
Adrián Flores-Romero ◽  
Vinnitsa Buzoianu-Anguiano ◽  
Elisa Garcia ◽  
Karla Soria-Zavala ◽  
...  

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