Regulation of nerve growth and patterning by cell surface protein disulphide isomerase

被引:48
作者
Cook, Geoffrey M. W. [1 ]
Sousa, Catia [1 ,2 ]
Schaeffer, Julia [1 ]
Wiles, Katherine [1 ]
Jareonsettasin, Prem [1 ,3 ]
Kalyanasundaram, Asanish [1 ,4 ]
Walder, Eleanor [1 ,4 ]
Casper, Catharina [1 ,5 ]
Patel, Serena [1 ,4 ]
Chua, Pei Wei [1 ,6 ]
Riboni-Verri, Gioia [1 ,7 ]
Raza, Mansoor [8 ]
Swaddiwudhipong, Nol [1 ]
Hui, Andrew [1 ]
Abdullah, Ameer [1 ]
Wajed, Saj [1 ,9 ]
Keynes, Roger J. [1 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[2] Grenoble Inst Neurosci, La Tronche, France
[3] Exeter Coll, Oxford, England
[4] Cambridge Univ Hosp, Sch Clin Med, Cambridge, England
[5] Winter Brandl Furniss Hubner Ross Kaiser & Polte, Patent & Rechtsanwaltskanzlei, Munich, Germany
[6] Monash Univ, Sch Med & Hlth Sci, Bandar Sunway, Malaysia
[7] Univ Aberdeen, Sch Med Med Sci & Nutr, Aberdeen, Scotland
[8] Cambridge Innovat Capital, Cambridge, England
[9] Univ Exeter, Med Sch, Exeter, Devon, England
来源
ELIFE | 2020年 / 9卷
基金
英国医学研究理事会;
关键词
NEURAL CREST MIGRATION; NITRIC-OXIDE; S-NITROSOTHIOLS; CONE COLLAPSE; ROSTRAL HALF; MOTOR AXONS; TRUNK; EXPRESSION; GUIDANCE; BINDING;
D O I
10.7554/eLife.54612
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Contact repulsion of growing axons is an essential mechanism for spinal nerve patterning. In birds and mammals the embryonic somites generate a linear series of impenetrable barriers, forcing axon growth cones to traverse one half of each somite as they extend towards their body targets. This study shows that protein disulphide isomerase provides a key component of these barriers, mediating contact repulsion at the cell surface in chick half-somites. Repulsion is reduced both in vivo and in vitro by a range of methods that inhibit enzyme activity. The activity is critical in initiating a nitric oxide/S-nitrosylation-dependent signal transduction pathway that regulates the growth cone cytoskeleton. Rat forebrain grey matter extracts contain a similar activity, and the enzyme is expressed at the surface of cultured human astrocytic cells and rat cortical astrocytes. We suggest this system is co-opted in the brain to counteract and regulate aberrant nerve terminal growth.
引用
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页码:1 / 27
页数:27
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