» Articles » PMID: 21551077

In Utero Electroporation As a Tool for Genetic Manipulation in Vivo to Study Psychiatric Disorders: from Genes to Circuits and Behaviors

Overview
Journal Neuroscientist
Publisher Sage Publications
Specialty Neurology
Date 2011 May 10
PMID 21551077
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

Many genetic risk factors for major mental disorders have key roles in brain development. Thus, exploring the roles for these genetic factors for brain development at the molecular, cellular, and neuronal circuit level is crucial for discovering how genetic disturbances affect high brain functions, which ultimately lead to disease pathologies. However, it is a tremendously difficult task, given that most mental disorders have genetic complexities in which many genetic risk factors have multiple roles in different cell types and brain regions over a time-course dependent manner. Furthermore, some genetic risk factors are likely to act epistatically in common molecular pathways. For this reason, a technique for spatial and temporal manipulation of multiple genes is necessary for understanding how genetic disturbances contribute to disease etiology. Here, the authors will review the said technique, in utero electroporation, which investigates the molecular disease pathways in rodent models for major mental disorders. This technique is also useful to examine the effect of genetic risks at the behavioral level. Furthermore, the authors will discuss the recent progress of this technology, such as inducible and cell type-specific targeting, as well as nonepisomal genetic manipulation, which provide further availability of this technique for research on major mental disorders.

Citing Articles

regulates stemness maintenance of radial glial cells and neuronal migration in the developing mouse cerebral cortex.

Liu J, Li H, Zhang Y Front Cell Neurosci. 2022; 16:865681.

PMID: 36313621 PMC: 9608153. DOI: 10.3389/fncel.2022.865681.


[Establishment of a system for regulating the gene expression of embryonic mouse cerebral cortex neural stem cells by electroporation].

Ou W, He L, Wang X, Yang X, Wang G, Li B Zhongguo Dang Dai Er Ke Za Zhi. 2022; 24(9):1061-1067.

PMID: 36111727 PMC: 9495236. DOI: 10.7499/j.issn.1008-8830.2204096.


In Utero Electroporation for Manipulation of Specific Neuronal Populations.

Yamashiro K, Ikegaya Y, Matsumoto N Membranes (Basel). 2022; 12(5).

PMID: 35629839 PMC: 9147339. DOI: 10.3390/membranes12050513.


Genetically encoded fluorescent sensors for imaging neuronal dynamics in vivo.

Day-Cooney J, Dalangin R, Zhong H, Mao T J Neurochem. 2022; 164(3):284-308.

PMID: 35285522 PMC: 11322610. DOI: 10.1111/jnc.15608.


RapID Cell Counter: Semi-Automated and Mid-Throughput Estimation of Cell Density within Diverse Cortical Layers.

Sekar A, Sanches T, Hino K, Kumar M, Wang J, Ha E eNeuro. 2021; 8(6).

PMID: 34725102 PMC: 8638678. DOI: 10.1523/ENEURO.0185-21.2021.


References
1.
Potvin S, Stip E, Sepehry A, Gendron A, Bah R, Kouassi E . Inflammatory cytokine alterations in schizophrenia: a systematic quantitative review. Biol Psychiatry. 2007; 63(8):801-8. DOI: 10.1016/j.biopsych.2007.09.024. View

2.
Madisen L, Zwingman T, Sunkin S, Oh S, Zariwala H, Gu H . A robust and high-throughput Cre reporting and characterization system for the whole mouse brain. Nat Neurosci. 2009; 13(1):133-40. PMC: 2840225. DOI: 10.1038/nn.2467. View

3.
Davidson B, Breakefield X . Viral vectors for gene delivery to the nervous system. Nat Rev Neurosci. 2003; 4(5):353-64. DOI: 10.1038/nrn1104. View

4.
Kamiya A, Kubo K, Tomoda T, Takaki M, Youn R, Ozeki Y . A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development. Nat Cell Biol. 2005; 7(12):1167-78. DOI: 10.1038/ncb1328. View

5.
Rapoport J, Addington A, Frangou S, Psych M . The neurodevelopmental model of schizophrenia: update 2005. Mol Psychiatry. 2005; 10(5):434-49. DOI: 10.1038/sj.mp.4001642. View