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@article{224936add7ff4c76a04ad5c184e1125e,
title = "Expression Pattern of Trace Amine-Associated Receptors during Differentiation of Human Pluripotent Stem Cells to Dopaminergic Neurons",
abstract = "Trace amine-associated receptors (TAARs), which were discovered only in 2001, are known to be involved in the regulation of a spectrum of neuronal processes and may play a role in the pathogenesis of a number of neuropsychiatric diseases, such as schizophrenia and others. We have previously shown that TAARs also have interconnections with the regulation of neurogenesis and, in particular, with the neurogenesis of dopamine neurons, but the exact mechanisms of this are still unknown. In our work we analyzed the expression of TAARs (TAAR1, TAAR2, TAAR5, TAAR6, TAAR8 and TAAR9) in cells from the human substantia nigra and ventral tegmental areas and in human pluripotent stem cells at consecutive stages of their differentiation to dopaminergic neurons, using RNA sequencing data from open databases, and TaqMan PCR data from the differentiation of human induced pluripotent stem cells in vitro. Detectable levels of TAARs expression were found in cells at the pluripotent stages, and the dynamic of their expression had a trend of increasing with the differentiation and maturation of dopamine neurons. The expression of several TAAR types (particularly TAAR5) was also found in human dopaminergic neuron-enriched zones in the midbrain. This is the first evidence of TAARs expression during neuronal differentiation, which can help to approach an understanding of the role of TAARs in neurogenesis.",
keywords = "Amines/metabolism, Cell Differentiation/genetics, Dopaminergic Neurons/metabolism, Humans, Induced Pluripotent Stem Cells/metabolism, Pluripotent Stem Cells/metabolism, Receptors, G-Protein-Coupled/genetics, trace amine-associated receptors (TAARs), dopamine (DA), neurogenesis, human induced pluripotent stem cells (human IPSCs), neuronal differentiation",
author = "Католикова, {Наталия Викторовна} and Ваганова, {Анастасия Николаевна} and Шафранская, {Дарья Дмитриевна} and Ефимова, {Евгения Викторовна} and Малашичева, {Анна Борисовна} and Гайнетдинов, {Рауль Радикович}",
year = "2023",
month = oct,
day = "18",
doi = "10.3390/ijms242015313",
language = "English",
volume = "24",
journal = "International Journal of Molecular Sciences",
issn = "1422-0067",
publisher = "MDPI AG",
number = "20",

}

RIS

TY - JOUR

T1 - Expression Pattern of Trace Amine-Associated Receptors during Differentiation of Human Pluripotent Stem Cells to Dopaminergic Neurons

AU - Католикова, Наталия Викторовна

AU - Ваганова, Анастасия Николаевна

AU - Шафранская, Дарья Дмитриевна

AU - Ефимова, Евгения Викторовна

AU - Малашичева, Анна Борисовна

AU - Гайнетдинов, Рауль Радикович

PY - 2023/10/18

Y1 - 2023/10/18

N2 - Trace amine-associated receptors (TAARs), which were discovered only in 2001, are known to be involved in the regulation of a spectrum of neuronal processes and may play a role in the pathogenesis of a number of neuropsychiatric diseases, such as schizophrenia and others. We have previously shown that TAARs also have interconnections with the regulation of neurogenesis and, in particular, with the neurogenesis of dopamine neurons, but the exact mechanisms of this are still unknown. In our work we analyzed the expression of TAARs (TAAR1, TAAR2, TAAR5, TAAR6, TAAR8 and TAAR9) in cells from the human substantia nigra and ventral tegmental areas and in human pluripotent stem cells at consecutive stages of their differentiation to dopaminergic neurons, using RNA sequencing data from open databases, and TaqMan PCR data from the differentiation of human induced pluripotent stem cells in vitro. Detectable levels of TAARs expression were found in cells at the pluripotent stages, and the dynamic of their expression had a trend of increasing with the differentiation and maturation of dopamine neurons. The expression of several TAAR types (particularly TAAR5) was also found in human dopaminergic neuron-enriched zones in the midbrain. This is the first evidence of TAARs expression during neuronal differentiation, which can help to approach an understanding of the role of TAARs in neurogenesis.

AB - Trace amine-associated receptors (TAARs), which were discovered only in 2001, are known to be involved in the regulation of a spectrum of neuronal processes and may play a role in the pathogenesis of a number of neuropsychiatric diseases, such as schizophrenia and others. We have previously shown that TAARs also have interconnections with the regulation of neurogenesis and, in particular, with the neurogenesis of dopamine neurons, but the exact mechanisms of this are still unknown. In our work we analyzed the expression of TAARs (TAAR1, TAAR2, TAAR5, TAAR6, TAAR8 and TAAR9) in cells from the human substantia nigra and ventral tegmental areas and in human pluripotent stem cells at consecutive stages of their differentiation to dopaminergic neurons, using RNA sequencing data from open databases, and TaqMan PCR data from the differentiation of human induced pluripotent stem cells in vitro. Detectable levels of TAARs expression were found in cells at the pluripotent stages, and the dynamic of their expression had a trend of increasing with the differentiation and maturation of dopamine neurons. The expression of several TAAR types (particularly TAAR5) was also found in human dopaminergic neuron-enriched zones in the midbrain. This is the first evidence of TAARs expression during neuronal differentiation, which can help to approach an understanding of the role of TAARs in neurogenesis.

KW - Amines/metabolism

KW - Cell Differentiation/genetics

KW - Dopaminergic Neurons/metabolism

KW - Humans

KW - Induced Pluripotent Stem Cells/metabolism

KW - Pluripotent Stem Cells/metabolism

KW - Receptors, G-Protein-Coupled/genetics

KW - trace amine-associated receptors (TAARs)

KW - dopamine (DA)

KW - neurogenesis

KW - human induced pluripotent stem cells (human IPSCs)

KW - neuronal differentiation

UR - https://www.mendeley.com/catalogue/043eeb4e-8ba2-381d-89f2-c86e7f2e6640/

U2 - 10.3390/ijms242015313

DO - 10.3390/ijms242015313

M3 - Article

C2 - 37894992

VL - 24

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1422-0067

IS - 20

M1 - 15313

ER -

ID: 114967033