Journal article icon

Journal article

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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

Actions


Access Document


Publisher copy:
10.1002/cne.24373

Authors


More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Pharmacology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Pharmacology
Role:
Author


More from this funder
Funding agency for:
Garas, F
Kormann, E
Magill, P
Sharott, A
Grant:
MC_UU_12020/5 and MC_UU_12024/2
MC_UU_12024/1
MC_UU_12024/1 to A.S.
More from this funder
Grant:
Marie Curie European Re-integration Grant (SNAP-PD)
More from this funder
Funding agency for:
Garas, F
Kormann, E


Publisher:
Wiley
Journal:
Journal of Comparative Neurology More from this journal
Volume:
526
Issue:
5
Pages:
877–898
Publication date:
2017-12-21
Acceptance date:
2017-11-29
DOI:
EISSN:
1096-9861
ISSN:
0021-9967


Keywords:
Pubs id:
pubs:809600
UUID:
uuid:2435f3a4-b656-4200-ba07-73c4cbbf4e86
Local pid:
pubs:809600
Deposit date:
2017-12-06

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP