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Minor changes in erythrocyte osmotic fragility in trace amine-associated receptor 5 (Taar5) knockout mice. / Zhukov, Ilya S.; Kubarskaya, Larisa G.; Karpova, Inessa V.; Vaganova, Anastasia N.; Karpenko, Marina N.; Gainetdinov, Raul R.

In: International Journal of Molecular Sciences, Vol. 22, No. 14, 7307, 07.07.2021.

Research output: Contribution to journalArticlepeer-review

Harvard

Zhukov, IS, Kubarskaya, LG, Karpova, IV, Vaganova, AN, Karpenko, MN & Gainetdinov, RR 2021, 'Minor changes in erythrocyte osmotic fragility in trace amine-associated receptor 5 (Taar5) knockout mice', International Journal of Molecular Sciences, vol. 22, no. 14, 7307. https://doi.org/10.3390/ijms22147307

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Vancouver

Author

Zhukov, Ilya S. ; Kubarskaya, Larisa G. ; Karpova, Inessa V. ; Vaganova, Anastasia N. ; Karpenko, Marina N. ; Gainetdinov, Raul R. / Minor changes in erythrocyte osmotic fragility in trace amine-associated receptor 5 (Taar5) knockout mice. In: International Journal of Molecular Sciences. 2021 ; Vol. 22, No. 14.

BibTeX

@article{83dd3142fa1d4ee389a933119d58d88e,
title = "Minor changes in erythrocyte osmotic fragility in trace amine-associated receptor 5 (Taar5) knockout mice",
abstract = "Trace amine-associated receptors (TAARs) are a group of G protein-coupled receptors that are expressed in the olfactory epithelium, central nervous system, and periphery. TAAR family generally consists of nine types of receptors (TAAR1-9), which can detect biogenic amines. During the last 5 years, the TAAR5 receptor became one of the most intriguing receptors in this subfamily. Recent studies revealed that TAAR5 is involved not only in sensing socially relevant odors but also in the regulation of dopamine and serotonin transmission, emotional regulation, and adult neurogenesis by providing significant input from the olfactory system to the limbic brain areas. Such results indicate that future antagonistic TAAR5-based therapies may have high pharmacological potential in the field of neuropsychiatric disorders. TAAR5 is known to be expressed in leucocytes as well. To evaluate potential hematological side effects of such future treatments we analyzed several hematological parameters in mice lacking TAAR5. In these mutants, we observed minor but significant changes in the osmotic fragility test of erythrocytes and hematocrit levels. At the same time, analysis of other parameters including complete blood count and reticulocyte levels showed no significant alterations in TAAR5 knockout mice. Thus, TAAR5 gene knockout leads to minor negative changes in the erythropoiesis or eryptosis processes, and further research in that field is needed. The impact of TAAR5 deficiency on other hematological parameters seems minimal. Such negative, albeit minor, effects of TAAR5 deficiency should be taken into account during future TAAR5-based therapy development.",
keywords = "Animal knockout model, Erythrocyte fragility, GPCR, Hematology, TAAR, TAAR5, Trace amine-associated receptor, Trace amines, Animal knockout model, Erythrocyte fragility, GPCR, Hematology, TAAR, TAAR5, Trace amine-associated receptor, Trace amines, MECHANISMS, trace amines, hematology, animal knockout model, trace amine-associated receptor, erythrocyte fragility, CELL",
author = "Zhukov, {Ilya S.} and Kubarskaya, {Larisa G.} and Karpova, {Inessa V.} and Vaganova, {Anastasia N.} and Karpenko, {Marina N.} and Gainetdinov, {Raul R.}",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = jul,
day = "7",
doi = "10.3390/ijms22147307",
language = "English",
volume = "22",
journal = "International Journal of Molecular Sciences",
issn = "1422-0067",
publisher = "MDPI AG",
number = "14",

}

RIS

TY - JOUR

T1 - Minor changes in erythrocyte osmotic fragility in trace amine-associated receptor 5 (Taar5) knockout mice

AU - Zhukov, Ilya S.

AU - Kubarskaya, Larisa G.

AU - Karpova, Inessa V.

AU - Vaganova, Anastasia N.

AU - Karpenko, Marina N.

AU - Gainetdinov, Raul R.

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

PY - 2021/7/7

Y1 - 2021/7/7

N2 - Trace amine-associated receptors (TAARs) are a group of G protein-coupled receptors that are expressed in the olfactory epithelium, central nervous system, and periphery. TAAR family generally consists of nine types of receptors (TAAR1-9), which can detect biogenic amines. During the last 5 years, the TAAR5 receptor became one of the most intriguing receptors in this subfamily. Recent studies revealed that TAAR5 is involved not only in sensing socially relevant odors but also in the regulation of dopamine and serotonin transmission, emotional regulation, and adult neurogenesis by providing significant input from the olfactory system to the limbic brain areas. Such results indicate that future antagonistic TAAR5-based therapies may have high pharmacological potential in the field of neuropsychiatric disorders. TAAR5 is known to be expressed in leucocytes as well. To evaluate potential hematological side effects of such future treatments we analyzed several hematological parameters in mice lacking TAAR5. In these mutants, we observed minor but significant changes in the osmotic fragility test of erythrocytes and hematocrit levels. At the same time, analysis of other parameters including complete blood count and reticulocyte levels showed no significant alterations in TAAR5 knockout mice. Thus, TAAR5 gene knockout leads to minor negative changes in the erythropoiesis or eryptosis processes, and further research in that field is needed. The impact of TAAR5 deficiency on other hematological parameters seems minimal. Such negative, albeit minor, effects of TAAR5 deficiency should be taken into account during future TAAR5-based therapy development.

AB - Trace amine-associated receptors (TAARs) are a group of G protein-coupled receptors that are expressed in the olfactory epithelium, central nervous system, and periphery. TAAR family generally consists of nine types of receptors (TAAR1-9), which can detect biogenic amines. During the last 5 years, the TAAR5 receptor became one of the most intriguing receptors in this subfamily. Recent studies revealed that TAAR5 is involved not only in sensing socially relevant odors but also in the regulation of dopamine and serotonin transmission, emotional regulation, and adult neurogenesis by providing significant input from the olfactory system to the limbic brain areas. Such results indicate that future antagonistic TAAR5-based therapies may have high pharmacological potential in the field of neuropsychiatric disorders. TAAR5 is known to be expressed in leucocytes as well. To evaluate potential hematological side effects of such future treatments we analyzed several hematological parameters in mice lacking TAAR5. In these mutants, we observed minor but significant changes in the osmotic fragility test of erythrocytes and hematocrit levels. At the same time, analysis of other parameters including complete blood count and reticulocyte levels showed no significant alterations in TAAR5 knockout mice. Thus, TAAR5 gene knockout leads to minor negative changes in the erythropoiesis or eryptosis processes, and further research in that field is needed. The impact of TAAR5 deficiency on other hematological parameters seems minimal. Such negative, albeit minor, effects of TAAR5 deficiency should be taken into account during future TAAR5-based therapy development.

KW - Animal knockout model

KW - Erythrocyte fragility

KW - GPCR

KW - Hematology

KW - TAAR

KW - TAAR5

KW - Trace amine-associated receptor

KW - Trace amines

KW - Animal knockout model

KW - Erythrocyte fragility

KW - GPCR

KW - Hematology

KW - TAAR

KW - TAAR5

KW - Trace amine-associated receptor

KW - Trace amines

KW - MECHANISMS

KW - trace amines

KW - hematology

KW - animal knockout model

KW - trace amine-associated receptor

KW - erythrocyte fragility

KW - CELL

UR - http://www.scopus.com/inward/record.url?scp=85109072871&partnerID=8YFLogxK

U2 - 10.3390/ijms22147307

DO - 10.3390/ijms22147307

M3 - Article

AN - SCOPUS:85109072871

VL - 22

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1422-0067

IS - 14

M1 - 7307

ER -

ID: 78836147