Hepatocyte growth factor promotes endogenous repair and functional recovery after spinal cord injury

2007 ◽  
Vol 85 (11) ◽  
pp. 2332-2342 ◽  
Author(s):  
Kazuya Kitamura ◽  
Akio Iwanami ◽  
Masaya Nakamura ◽  
Junichi Yamane ◽  
Kota Watanabe ◽  
...  
PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e27706 ◽  
Author(s):  
Kazuya Kitamura ◽  
Kanehiro Fujiyoshi ◽  
Jun-ichi Yamane ◽  
Fumika Toyota ◽  
Keigo Hikishima ◽  
...  

2019 ◽  
Vol 20 (23) ◽  
pp. 6078 ◽  
Author(s):  
Kentaro Yamane ◽  
Haruo Misawa ◽  
Tomoyuki Takigawa ◽  
Yoshihiro Ito ◽  
Toshifumi Ozaki ◽  
...  

Spinal cord injury (SCI) results in neural tissue loss and so far untreatable functional impairment. In addition, at the initial injury site, inflammation induces secondary damage, and glial scar formation occurs to limit inflammation-mediated tissue damage. Consequently, it obstructs neural regeneration. Many studies have been conducted in the field of SCI; however, no satisfactory treatment has been established to date. Hepatocyte growth factor (HGF) is one of the neurotrophic growth factors and has been listed as a candidate medicine for SCI treatment. The highlighted effects of HGF on neural regeneration are associated with its anti-inflammatory and anti-fibrotic activities. Moreover, HGF exerts positive effects on transplanted stem cell differentiation into neurons. This paper reviews the mechanisms underlying the therapeutic effects of HGF in SCI recovery, and introduces recent advances in the clinical applications of HGF therapy.


2019 ◽  
Vol 20 (5) ◽  
pp. 1054 ◽  
Author(s):  
Kazuya Kitamura ◽  
Narihito Nagoshi ◽  
Osahiko Tsuji ◽  
Morio Matsumoto ◽  
Hideyuki Okano ◽  
...  

Hepatocyte growth factor (HGF) was first identified as a potent mitogen for mature hepatocytes, and has also gained attention as a strong neurotrophic factor in the central nervous system. We found that during the acute phase of spinal cord injury (SCI) in rats, c-Met, the specific receptor for HGF, increases sharply, while the endogenous HGF up-regulation is relatively weak. Introducing exogenous HGF into the spinal cord by injecting an HGF-expressing viral vector significantly increased the neuron and oligodendrocyte survival, angiogenesis, and axonal regeneration, to reduce the area of damage and to promote functional recovery in rats after SCI. Other recent studies in rodents have shown that exogenously administered HGF during the acute phase of SCI reduces astrocyte activation to decrease glial scar formation, and exerts anti-inflammatory effects to reduce leukocyte infiltration. We also reported that the intrathecal infusion of recombinant human HGF (intrathecal rhHGF) improves neurological hand function after cervical contusive SCI in the common marmoset, a non-human primate. Based on these collective results, we conducted a phase I/II clinical trial of intrathecal rhHGF for patients with acute cervical SCI who showed a modified Frankel grade of A/B1/B2 72 h after injury onset, from June 2014 to May 2018.


2012 ◽  
Vol 233 (1) ◽  
pp. 312-322 ◽  
Author(s):  
Soo Ryeong Jeong ◽  
Min Jung Kwon ◽  
Hwan Goo Lee ◽  
Eun Hye Joe ◽  
Jae Ho Lee ◽  
...  

2007 ◽  
Vol 1151 ◽  
pp. 188-194 ◽  
Author(s):  
Munehisa Shimamura ◽  
Naoyuki Sato ◽  
Masataka Sata ◽  
Kouji Wakayama ◽  
Toshio Ogihara ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Sipin Zhu ◽  
Yibo Ying ◽  
Lin Ye ◽  
Weiyang Ying ◽  
Jiahui Ye ◽  
...  

Protecting the death of nerve cells is an essential tactic for spinal cord injury (SCI) repair. Recent studies show that nerve growth factors can reduce the death of nerve cells and promote the healing of nerve injury. To investigate the conducive effect of fibroblast growth factor 21 (FGF21) on SCI repair. FGF21 proteins were systemically delivered into rat model of SCI via tail vein injection. We found that administration of FGF21 significantly promoted the functional recovery of SCI as assessed by BBB scale and inclined plane test, and attenuated cell death in the injured area by histopathological examination with Nissl staining. This was accompanied with increased expression of NeuN, GAP43 and NF200, and deceased expression of GFAP. Interestingly, FGF21 was found to attenuate the elevated expression level of the autophagy marker LC3-II (microtubules associated protein 1 light chain 3-II) induced by SCI in a dose-dependent manner. These data show that FGF21 promotes the functional recovery of SCI via restraining injury-induced cell autophagy, suggesting that systemic administration of FGF21 could have a therapeutic potential for SCI repair.


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