Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system

Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circu...
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Autor*in:	Gamlin, Clare R. [verfasserIn] Yu, Wan-Qing Wong, Rachel O. L. Hoon, Mrinalini

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2018

Schlagwörter:	Inhibition Synaptic targeting Synapse formation Circuit refinement Synapse maturation

Anmerkung:	© The Author(s). 2018

Übergeordnetes Werk:	Enthalten in: Neural development - London : BioMed Central, 2006, 13(2018), 1 vom: 07. Juni
Übergeordnetes Werk:	volume:13 ; year:2018 ; number:1 ; day:07 ; month:06

Links:	Volltext

DOI / URN:	10.1186/s13064-018-0109-6

Katalog-ID:	SPR030123127

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520			\|a Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition.
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allfields	10.1186/s13064-018-0109-6 doi (DE-627)SPR030123127 (SPR)s13064-018-0109-6-e DE-627 ger DE-627 rakwb eng Gamlin, Clare R. verfasserin aut Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213 Yu, Wan-Qing aut Wong, Rachel O. L. aut Hoon, Mrinalini (orcid)0000-0002-3590-8743 aut Enthalten in Neural development London : BioMed Central, 2006 13(2018), 1 vom: 07. Juni (DE-627)519199669 (DE-600)2254847-6 1749-8104 nnns volume:13 year:2018 number:1 day:07 month:06 https://dx.doi.org/10.1186/s13064-018-0109-6 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2018 1 07 06
spelling	10.1186/s13064-018-0109-6 doi (DE-627)SPR030123127 (SPR)s13064-018-0109-6-e DE-627 ger DE-627 rakwb eng Gamlin, Clare R. verfasserin aut Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213 Yu, Wan-Qing aut Wong, Rachel O. L. aut Hoon, Mrinalini (orcid)0000-0002-3590-8743 aut Enthalten in Neural development London : BioMed Central, 2006 13(2018), 1 vom: 07. Juni (DE-627)519199669 (DE-600)2254847-6 1749-8104 nnns volume:13 year:2018 number:1 day:07 month:06 https://dx.doi.org/10.1186/s13064-018-0109-6 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2018 1 07 06
allfields_unstemmed	10.1186/s13064-018-0109-6 doi (DE-627)SPR030123127 (SPR)s13064-018-0109-6-e DE-627 ger DE-627 rakwb eng Gamlin, Clare R. verfasserin aut Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213 Yu, Wan-Qing aut Wong, Rachel O. L. aut Hoon, Mrinalini (orcid)0000-0002-3590-8743 aut Enthalten in Neural development London : BioMed Central, 2006 13(2018), 1 vom: 07. Juni (DE-627)519199669 (DE-600)2254847-6 1749-8104 nnns volume:13 year:2018 number:1 day:07 month:06 https://dx.doi.org/10.1186/s13064-018-0109-6 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2018 1 07 06
allfieldsGer	10.1186/s13064-018-0109-6 doi (DE-627)SPR030123127 (SPR)s13064-018-0109-6-e DE-627 ger DE-627 rakwb eng Gamlin, Clare R. verfasserin aut Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213 Yu, Wan-Qing aut Wong, Rachel O. L. aut Hoon, Mrinalini (orcid)0000-0002-3590-8743 aut Enthalten in Neural development London : BioMed Central, 2006 13(2018), 1 vom: 07. Juni (DE-627)519199669 (DE-600)2254847-6 1749-8104 nnns volume:13 year:2018 number:1 day:07 month:06 https://dx.doi.org/10.1186/s13064-018-0109-6 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2018 1 07 06
allfieldsSound	10.1186/s13064-018-0109-6 doi (DE-627)SPR030123127 (SPR)s13064-018-0109-6-e DE-627 ger DE-627 rakwb eng Gamlin, Clare R. verfasserin aut Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213 Yu, Wan-Qing aut Wong, Rachel O. L. aut Hoon, Mrinalini (orcid)0000-0002-3590-8743 aut Enthalten in Neural development London : BioMed Central, 2006 13(2018), 1 vom: 07. Juni (DE-627)519199669 (DE-600)2254847-6 1749-8104 nnns volume:13 year:2018 number:1 day:07 month:06 https://dx.doi.org/10.1186/s13064-018-0109-6 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2018 1 07 06
language	English
source	Enthalten in Neural development 13(2018), 1 vom: 07. Juni volume:13 year:2018 number:1 day:07 month:06
sourceStr	Enthalten in Neural development 13(2018), 1 vom: 07. Juni volume:13 year:2018 number:1 day:07 month:06
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Inhibition Synaptic targeting Synapse formation Circuit refinement Synapse maturation
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container_title	Neural development
authorswithroles_txt_mv	Gamlin, Clare R. @@aut@@ Yu, Wan-Qing @@aut@@ Wong, Rachel O. L. @@aut@@ Hoon, Mrinalini @@aut@@
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author	Gamlin, Clare R.
spellingShingle	Gamlin, Clare R. misc Inhibition misc Synaptic targeting misc Synapse formation misc Circuit refinement misc Synapse maturation Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system
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topic_title	Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system Inhibition (dpeaa)DE-He213 Synaptic targeting (dpeaa)DE-He213 Synapse formation (dpeaa)DE-He213 Circuit refinement (dpeaa)DE-He213 Synapse maturation (dpeaa)DE-He213
topic	misc Inhibition misc Synaptic targeting misc Synapse formation misc Circuit refinement misc Synapse maturation
topic_unstemmed	misc Inhibition misc Synaptic targeting misc Synapse formation misc Circuit refinement misc Synapse maturation
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title	Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system
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title_full	Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system
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author_browse	Gamlin, Clare R. Yu, Wan-Qing Wong, Rachel O. L. Hoon, Mrinalini
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title_sort	assembly and maintenance of gabaergic and glycinergic circuits in the mammalian nervous system
title_auth	Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system
abstract	Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. © The Author(s). 2018
abstractGer	Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. © The Author(s). 2018
abstract_unstemmed	Abstract Inhibition in the central nervous systems (CNS) is mediated by two neurotransmitters: gamma-aminobutyric acid (GABA) and glycine. Inhibitory synapses are generally GABAergic or glycinergic, although there are synapses that co-release both neurotransmitter types. Compared to excitatory circuits, much less is known about the cellular and molecular mechanisms that regulate synaptic partner selection and wiring patterns of inhibitory circuits. Recent work, however, has begun to fill this gap in knowledge, providing deeper insight into whether GABAergic and glycinergic circuit assembly and maintenance rely on common or distinct mechanisms. Here we summarize and contrast the developmental mechanisms that regulate the selection of synaptic partners, and that promote the formation, refinement, maturation and maintenance of GABAergic and glycinergic synapses and their respective wiring patterns. We highlight how some parts of the CNS demonstrate developmental changes in the type of inhibitory transmitter or receptor composition at their inhibitory synapses. We also consider how perturbation of the development or maintenance of one type of inhibitory connection affects other inhibitory synapse types in the same circuit. Mechanistic insight into the development and maintenance of GABAergic and glycinergic inputs, and inputs that co-release both these neurotransmitters could help formulate comprehensive therapeutic strategies for treating disorders of synaptic inhibition. © The Author(s). 2018
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title_short	Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system
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Assembly and maintenance of GABAergic and Glycinergic circuits in the mammalian nervous system

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