scholarly journals ALS-Linked SOD1 Mutants Enhance Neurite Outgrowth and Branching in Adult Motor Neurons

iScience ◽  
2019 ◽  
Vol 19 ◽  
pp. 448-449
Author(s):  
Zachary Osking ◽  
Jacob I. Ayers ◽  
Ryan Hildebrandt ◽  
Kristen Skruber ◽  
Hilda Brown ◽  
...  
iScience ◽  
2019 ◽  
Vol 11 ◽  
pp. 294-304 ◽  
Author(s):  
Zachary Osking ◽  
Jacob I. Ayers ◽  
Ryan Hildebrandt ◽  
Kristen Skruber ◽  
Hilda Brown ◽  
...  

2009 ◽  
Vol 220 (2) ◽  
pp. 303-315 ◽  
Author(s):  
Jose V. Montoya G. ◽  
Jhon Jairo Sutachan ◽  
Wai Si Chan ◽  
Alexandra Sideris ◽  
Thomas J.J. Blanck ◽  
...  

2020 ◽  
Vol 117 (10) ◽  
pp. 3124-3135
Author(s):  
Ana M. Sandoval‐Castellanos ◽  
Frederik Claeyssens ◽  
John W. Haycock

2002 ◽  
Vol 20 (6) ◽  
pp. 521-526 ◽  
Author(s):  
Kwang‐Woo Lee ◽  
Hyun‐Jeong Kim ◽  
Jung‐Joon Sung ◽  
Kyung‐Seok Park ◽  
Manho Kim

2008 ◽  
Vol 181 (1) ◽  
pp. 37-41 ◽  
Author(s):  
Philip Van Damme ◽  
Annelies Van Hoecke ◽  
Diether Lambrechts ◽  
Peter Vanacker ◽  
Elke Bogaert ◽  
...  

Recently, mutations in the progranulin (PGRN) gene were found to cause familial and apparently sporadic frontotemporal lobe dementia (FTLD). Moreover, missense changes in PGRN were identified in patients with motor neuron degeneration, a condition that is related to FTLD. Most mutations identified in patients with FTLD until now have been null mutations. However, it remains unknown whether PGRN protein levels are reduced in the central nervous system from such patients. The effects of PGRN on neurons also remain to be established. We report that PGRN levels are reduced in the cerebrospinal fluid from FTLD patients carrying a PGRN mutation. We observe that PGRN and GRN E (one of the proteolytic fragments of PGRN) promote neuronal survival and enhance neurite outgrowth in cultured neurons. These results demonstrate that PGRN/GRN is a neurotrophic factor with activities that may be involved in the development of the nervous system and in neurodegeneration.


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