Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum

Calretinin-expressing (CR+) interneurons are the most common type of striatal interneuron in primates. However, because CR+ interneurons are relatively scarce in rodent striatum, little is known about their molecular and other properties, and they are typically excluded from models of striatal circu...

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Main Authors: Garas, F, Kormann, E, Shah, R, Vinciati, F, Smith, Y, Magill, P, Sharott, A
Format: Journal article
Published: Wiley 2017
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author Garas, F
Kormann, E
Shah, R
Vinciati, F
Smith, Y
Magill, P
Sharott, A
author_facet Garas, F
Kormann, E
Shah, R
Vinciati, F
Smith, Y
Magill, P
Sharott, A
author_sort Garas, F
collection OXFORD
description Calretinin-expressing (CR+) interneurons are the most common type of striatal interneuron in primates. However, because CR+ interneurons are relatively scarce in rodent striatum, little is known about their molecular and other properties, and they are typically excluded from models of striatal circuitry. Moreover, CR+ interneurons are often treated in models as a single homogenous population, despite previous descriptions of their heterogeneous structures and spatial distributions in rodents and primates. Here, we demonstrate that, in rodents, the combinatorial expression of secretagogin (Scgn), specificity protein 8 (SP8) and/or LIM homeobox protein 7 (Lhx7) separates striatal CR+ interneurons into 3 structurally- and topographically-distinct cell populations. The CR+/Scgn+/SP8+/Lhx7 interneurons are small-sized (typically 7-11 µm in somatic diameter), possess tortuous, partially-spiny dendrites, and are rostrally biased in their positioning within striatum. The CR+/Scgn/SP8/Lhx7interneurons are medium-sized (typically 12-15 µm), have bipolar dendrites, and are homogenously distributed throughout striatum. The CR+/Scgn/SP8/Lhx7+ interneurons are relatively large-sized (typically 12-20 µm), and have thick, infrequently-branching dendrites. Furthermore, we provide the first in vivo electrophysiological recordings of identified CR+ interneurons, all of which were the CR+/Scgn/SP8/Lhx7 cell type. In the primate striatum, Scgn co-expression also identified a topographically-distinct CR+ interneuron population with a rostral bias similar to that seen in both rats and mice. Taken together, these results suggest that striatal CR+ interneurons comprise at least three molecularly-, structurally- and topographically-distinct cell populations in rodents. These properties are partially conserved in primates, in which the relative abundance of CR+ interneurons suggests that they play a critical role in striatal microcircuits.
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spelling oxford-uuid:2435f3a4-b656-4200-ba07-73c4cbbf4e862022-03-26T11:48:43ZStructural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatumJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2435f3a4-b656-4200-ba07-73c4cbbf4e86Symplectic Elements at OxfordWiley2017Garas, FKormann, EShah, RVinciati, FSmith, YMagill, PSharott, ACalretinin-expressing (CR+) interneurons are the most common type of striatal interneuron in primates. However, because CR+ interneurons are relatively scarce in rodent striatum, little is known about their molecular and other properties, and they are typically excluded from models of striatal circuitry. Moreover, CR+ interneurons are often treated in models as a single homogenous population, despite previous descriptions of their heterogeneous structures and spatial distributions in rodents and primates. Here, we demonstrate that, in rodents, the combinatorial expression of secretagogin (Scgn), specificity protein 8 (SP8) and/or LIM homeobox protein 7 (Lhx7) separates striatal CR+ interneurons into 3 structurally- and topographically-distinct cell populations. The CR+/Scgn+/SP8+/Lhx7 interneurons are small-sized (typically 7-11 µm in somatic diameter), possess tortuous, partially-spiny dendrites, and are rostrally biased in their positioning within striatum. The CR+/Scgn/SP8/Lhx7interneurons are medium-sized (typically 12-15 µm), have bipolar dendrites, and are homogenously distributed throughout striatum. The CR+/Scgn/SP8/Lhx7+ interneurons are relatively large-sized (typically 12-20 µm), and have thick, infrequently-branching dendrites. Furthermore, we provide the first in vivo electrophysiological recordings of identified CR+ interneurons, all of which were the CR+/Scgn/SP8/Lhx7 cell type. In the primate striatum, Scgn co-expression also identified a topographically-distinct CR+ interneuron population with a rostral bias similar to that seen in both rats and mice. Taken together, these results suggest that striatal CR+ interneurons comprise at least three molecularly-, structurally- and topographically-distinct cell populations in rodents. These properties are partially conserved in primates, in which the relative abundance of CR+ interneurons suggests that they play a critical role in striatal microcircuits.
spellingShingle Garas, F
Kormann, E
Shah, R
Vinciati, F
Smith, Y
Magill, P
Sharott, A
Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title_full Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title_fullStr Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title_full_unstemmed Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title_short Structural and molecular heterogeneity of calretinin-expressing interneurons in the rodent and primate striatum
title_sort structural and molecular heterogeneity of calretinin expressing interneurons in the rodent and primate striatum
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