Cell fate determination, neuronal maintenance and disease state: The emerging role of transcription factors Lmx1a and Lmx1b
- PMID: 26526610
- DOI: 10.1016/j.febslet.2015.10.020
Cell fate determination, neuronal maintenance and disease state: The emerging role of transcription factors Lmx1a and Lmx1b
Abstract
LIM-homeodomain (LIM-HD) proteins are evolutionary conserved developmental transcription factors. LIM-HD Lmx1a and Lmx1b orchestrate complex temporal and spatial gene expression of the dopaminergic pathway, and evidence shows they are also involved in adult neuronal homeostasis. In this review, the multiple roles played by Lmx1a and Lmx1b will be discussed. Controlled Lmx1a and Lmx1b expression and activities ensure the proper formation of critical signaling centers, including the embryonic ventral mesencephalon floor plate and sharp boundaries between lineage-specific cells. Lmx1a and Lmx1b expression persists in mature dopaminergic neurons of the substantia nigra pars compacta and the ventral tegmental area, and their role in the adult brain is beginning to be revealed. Notably, LMX1B expression was lower in brain tissue affected by Parkinson's disease. Actual and future applications of Lmx1a and Lmx1b transcription factors in stem cell production as well as in direct conversion of fibroblast into dopaminergic neurons are also discussed. A thorough understanding of the role of LMX1A and LMX1B in a number of disease states, including developmental diseases, cancer and neurodegenerative diseases, could lead to significant benefits for human healthcare.
Keywords: Cancer; Neurodegeneration; Parkinson’s disease; Stem cell.
Copyright © 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Similar articles
-
Lmx1a and lmx1b function cooperatively to regulate proliferation, specification, and differentiation of midbrain dopaminergic progenitors.J Neurosci. 2011 Aug 31;31(35):12413-25. doi: 10.1523/JNEUROSCI.1077-11.2011. J Neurosci. 2011. PMID: 21880902 Free PMC article.
-
Dopaminergic control of autophagic-lysosomal function implicates Lmx1b in Parkinson's disease.Nat Neurosci. 2015 Jun;18(6):826-35. doi: 10.1038/nn.4004. Epub 2015 Apr 27. Nat Neurosci. 2015. PMID: 25915474
-
An Lmx1b-miR135a2 regulatory circuit modulates Wnt1/Wnt signaling and determines the size of the midbrain dopaminergic progenitor pool.PLoS Genet. 2013;9(12):e1003973. doi: 10.1371/journal.pgen.1003973. Epub 2013 Dec 12. PLoS Genet. 2013. PMID: 24348261 Free PMC article.
-
Molecular programming of stem cells into mesodiencephalic dopaminergic neurons.Trends Neurosci. 2006 Nov;29(11):601-3. doi: 10.1016/j.tins.2006.09.003. Epub 2006 Oct 9. Trends Neurosci. 2006. PMID: 17030431 Review.
-
The aetiology of idiopathic Parkinson's disease.Mol Pathol. 2001 Dec;54(6):369-80. Mol Pathol. 2001. PMID: 11724911 Free PMC article. Review.
Cited by
-
Transcription Factor Lmx1b Negatively Regulates Osteoblast Differentiation and Bone Formation.Int J Mol Sci. 2022 May 7;23(9):5225. doi: 10.3390/ijms23095225. Int J Mol Sci. 2022. PMID: 35563615 Free PMC article.
-
The Rate of Change in Alcohol Misuse Across Adolescence is Heritable.Alcohol Clin Exp Res. 2017 Jan;41(1):57-64. doi: 10.1111/acer.13262. Epub 2016 Nov 28. Alcohol Clin Exp Res. 2017. PMID: 27892595 Free PMC article.
-
Elevated COUP-TFII expression in dopaminergic neurons accelerates the progression of Parkinson's disease through mitochondrial dysfunction.PLoS Genet. 2020 Jun 24;16(6):e1008868. doi: 10.1371/journal.pgen.1008868. eCollection 2020 Jun. PLoS Genet. 2020. PMID: 32579581 Free PMC article.
-
Single-Cell RNA Analysis of Type I Spiral Ganglion Neurons Reveals a Lmx1a Population in the Cochlea.Front Mol Neurosci. 2020 May 25;13:83. doi: 10.3389/fnmol.2020.00083. eCollection 2020. Front Mol Neurosci. 2020. PMID: 32523514 Free PMC article.
-
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment.Hum Genet. 2018 Jul;137(6-7):471-478. doi: 10.1007/s00439-018-1899-7. Epub 2018 Jul 3. Hum Genet. 2018. PMID: 29971487 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous