» Articles » PMID: 22866028

Dopaminergic Axon Guidance: Which Makes What?

Overview
Specialty Cell Biology
Date 2012 Aug 7
PMID 22866028
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Mesotelencephalic pathways in the adult central nervous system have been studied in great detail because of their implication in major physiological functions as well as in psychiatric, neurological, and neurodegenerative diseases. However, the ontogeny of these pathways and the molecular mechanisms that guide dopaminergic axons during embryogenesis have been only recently studied. This line of research is of crucial interest for the repair of lesioned circuits in adulthood following neurodegenerative diseases or common traumatic injuries. For instance, in the adult, the anatomic and functional repair of the nigrostriatal pathway following dopaminergic embryonic neuron transplantation suggests that specific guidance cues exist which govern embryonic fibers outgrowth, and suggests that axons from transplanted embryonic cells are able to respond to theses cues, which then guide them to their final targets. In this review, we first synthesize the work that has been performed in the last few years on developing mesotelencephalic pathways, and summarize the current knowledge on the identity of cellular and molecular signals thought to be involved in establishing mesotelencephalic dopaminergic neuronal connectivity during embryogenesis in the central nervous system of rodents. Then, we review the modulation of expression of these molecular signals in the lesioned adult brain and discuss their potential role in remodeling the mesotelencephalic dopaminergic circuitry, with a particular focus on Parkinson's disease (PD). Identifying guidance molecules involved in the connection of grafted cells may be useful for cellular therapy in Parkinsonian patients, as these molecules may help direct axons from grafted cells along the long distance they have to travel from the substantia nigra to the striatum.

Citing Articles

Development, wiring and function of dopamine neuron subtypes.

Garritsen O, van Battum E, Grossouw L, Pasterkamp R Nat Rev Neurosci. 2023; 24(3):134-152.

PMID: 36653531 DOI: 10.1038/s41583-022-00669-3.


Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders.

Strafella C, Caputo V, Termine A, Fabrizio C, Ruffo P, Potenza S Front Neurol. 2021; 12:626066.

PMID: 34135841 PMC: 8200556. DOI: 10.3389/fneur.2021.626066.


Controllable fusion of human brain organoids using acoustofluidics.

Ao Z, Cai H, Wu Z, Ott J, Wang H, Mackie K Lab Chip. 2021; 21(4):688-699.

PMID: 33514983 PMC: 8464403. DOI: 10.1039/d0lc01141j.


Nolz1 expression is required in dopaminergic axon guidance and striatal innervation.

Soleilhavoup C, Travaglio M, Patrick K, Garcao P, Boobalan E, Adolfs Y Nat Commun. 2020; 11(1):3111.

PMID: 32561725 PMC: 7305235. DOI: 10.1038/s41467-020-16947-6.


Axonal Growth of Midbrain Dopamine Neurons is Modulated by the Cell Adhesion Molecule ALCAM Through -Heterophilic Interactions with L1cam, Chl1, and Semaphorins.

Bye C, Rytova V, Alsanie W, Parish C, Thompson L J Neurosci. 2019; 39(34):6656-6667.

PMID: 31300520 PMC: 6703882. DOI: 10.1523/JNEUROSCI.0278-19.2019.


References
1.
Goldshmit Y, Bourne J . Upregulation of EphA4 on astrocytes potentially mediates astrocytic gliosis after cortical lesion in the marmoset monkey. J Neurotrauma. 2010; 27(7):1321-32. DOI: 10.1089/neu.2010.1294. View

2.
Miyasaki J, Grimes D, Lang A . Acute delirium after withdrawal of amantadine in Parkinson's disease. Neurology. 1999; 52(8):1720-1. DOI: 10.1212/wnl.52.8.1717-d. View

3.
Tang M, Miyamoto Y, Huang E . Multiple roles of beta-catenin in controlling the neurogenic niche for midbrain dopamine neurons. Development. 2009; 136(12):2027-38. PMC: 2685724. DOI: 10.1242/dev.034330. View

4.
Tsuchiya R, Takahashi K, Liu F, Takahashi H . Aberrant axonal projections from mammillary bodies in Pax6 mutant mice: possible roles of Netrin-1 and Slit 2 in mammillary projections. J Neurosci Res. 2008; 87(7):1620-33. DOI: 10.1002/jnr.21966. View

5.
Kim J, Park S, Yang J, Shin E, Lee J, Yun J . SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population. J Hum Genet. 2010; 56(2):125-9. DOI: 10.1038/jhg.2010.130. View