4.5 Article

Phosphorylation of Collapsin Response Mediator Protein 1 (CRMP1) at Tyrosine 504 residue regulates Semaphorin 3A-induced cortical dendritic growth

Journal

JOURNAL OF NEUROCHEMISTRY
Volume 157, Issue 4, Pages 1207-1221

Publisher

WILEY
DOI: 10.1111/jnc.15304

Keywords

cortical neuron; CRMP1; dendritic growth; Fyn; Sema3A; tyrosine phosphorylation

Funding

  1. Japan Society for the Promotion of Science (JSPS) [16K07062]
  2. JSPS [20K15937]
  3. fund for Creation of Innovation Centers for Advanced Interdisciplinary Research Areas Program in the Project for Developing Innovation Systems from the MEXT
  4. Grants-in-Aid for Scientific Research [16K07062, 20K15937] Funding Source: KAKEN

Ask authors/readers for more resources

Phosphorylation of CRMP1 at residue Tyr504 by Fyn is critical for Sema3A-regulated dendritic development of cortical pyramidal neurons. Fyn phosphorylates CRMP1, leading to an increase in phosphotyrosine signal in growth cones upon Sema3A stimulation. Mutant CRMP1-Tyr504Phe suppresses Sema3A-induced growth cone collapse and dendritic growth in mouse neurons.
Collapsin response mediator proteins (CRMPs) have been identified as mediating proteins of repulsive axon guidance cue Semaphorin-3A (Sema3A). Phosphorylation of CRMPs plays a crucial role in the Sema3A signaling cascade. It has been shown that Fyn phosphorylates CRMP1 at Tyrosine 504 residue (Tyr504); however, the physiological role of this phosphorylation has not been examined. We found that CRMP1 was the most strongly phosphorylated by Fyn among the five members of CRMPs. We confirmed Tyr504 phosphorylation of CRMP1 by Fyn. Immunocytochemistry of mouse dorsal root ganglion (DRG) neurons showed that phosphotyrosine signal in the growth cones was transiently increased in the growth cones upon Sema3A stimulation. Tyr504-phosphorylated CRMP1 also tended to increase after Sema3A simulation. Ectopic expression of a single amino acid mutant of CRMP1 replacing Tyr504 with phenylalanine (CRMP1-Tyr504Phe) suppressed Sema3A-induced growth cone collapse response in chick DRG neurons. CRMP1-Tyr504Phe expression in mouse hippocampal neurons also suppressed Sema3A but not Sema3F-induced growth cone collapse response. Immunohistochemistry showed that Tyr504-phosphorylated CRMP1 was present in the cell bodies and in the dendritic processes of mouse cortical neurons. CRMP1-Tyr504Phe suppressed Sema3A-induced dendritic growth of primary cultured mouse cortical neurons as well as the dendritic development of cortical pyramidal neurons in vivo. Fyn(+/-); Crmp1(+/-) double heterozygous mutant mice exhibited poor development of cortical layer V basal dendrites, which was the similar phenotype observed in Sema3a(-/-), Fyn(-/-), and Crmp1(-/-) mice. These findings demonstrate that Tyr504 phosphorylation of CRMP1 by Fyn is an essential step of Sema3A-regulated dendritic development of cortical pyramidal neurons. (247 words).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available