Jimpy Mice: Quantitation of Myelin-Associated Glycoprotein and Other Proteins

2006 ◽  
Vol 47 (1) ◽  
pp. 322-325 ◽  
Author(s):  
Katsuhiko Yanagisawa ◽  
Richard H. Quarles
2001 ◽  
Vol 106 (3) ◽  
pp. 130-132 ◽  
Author(s):  
M. Donfrid ◽  
S. Apostolski ◽  
N. Suvajdžić ◽  
G. Janković ◽  
V. Čemerikić-Martinović ◽  
...  

1988 ◽  
Vol 51 (5) ◽  
pp. 1646-1650 ◽  
Author(s):  
Arrel D. Toews ◽  
Francis V. White ◽  
Pierre Morell

1991 ◽  
Vol 57 (1) ◽  
pp. 318-322 ◽  
Author(s):  
William P. Bartlett ◽  
Xiao-Su Li ◽  
James R. Connor
Keyword(s):  

2013 ◽  
Vol 288 (29) ◽  
pp. 20837-20842 ◽  
Author(s):  
Steven J. Henle ◽  
Lucas P. Carlstrom ◽  
Thomas R. Cheever ◽  
John R. Henley

Negatively targeting the tumor suppressor and phosphoinositide phosphatase PTEN (phosphatase and tensin homologue) promotes axon regrowth after injury. How PTEN functions in axon guidance has remained unknown. Here we report the differential role of PTEN in chemotactic guidance of axonal growth cones. Down-regulating PTEN expression in Xenopus laevis spinal neurons selectively abolished growth cone chemorepulsion but permitted chemoattraction. These findings persisted during cAMP-dependent switching of turning behaviors. Live cell imaging using a GFP biosensor revealed rapid PTEN-dependent depression of phosphatidylinositol 3,4,5-trisphosphate levels in the growth cone induced by the repellent myelin-associated glycoprotein. Moreover, down-regulating PTEN expression blocked negative remodeling of β1-integrin adhesions triggered by myelin-associated glycoprotein, yet permitted integrin clustering by a positive chemotropic treatment. Thus, PTEN negatively regulates growth cone phosphatidylinositol 3,4,5-trisphosphate levels and mediates chemorepulsion, whereas chemoattraction is PTEN-independent. Regenerative therapies targeting PTEN may therefore suppress growth cone repulsion to soluble cues while permitting attractive guidance, an essential feature for re-forming functional neural circuits.


1977 ◽  
Vol 163 (3) ◽  
pp. 635-637 ◽  
Author(s):  
R H Quarles ◽  
C F Pasnak

Treatment of the chloroform/methanol-insoluble residue of rat brain myelin with lithium 3,5-di-iodosalicylate solubilized the major myelin-associated glycoprotein along with most other proteins and glycoproteins. Equilibration of the extract with phenol resulted in the selective partitioning of the major glycoprotein into the aqueous phase, whereas nearly all of the other proteins and glycoproteins went into the phenol phase.


Author(s):  
D. Johnson ◽  
S. Sato ◽  
R. H. Quarles ◽  
H. deF. Webster ◽  
R. O. Brady

Sign in / Sign up

Export Citation Format

Share Document