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

• Type of Material: Article
• Authors: Farid N. Garas, University of Oxford; Eszter Kormann, University of Oxford; Rahul S. Shah, University of Oxford; Federica Vinciati, University of Oxford; Yoland Smith, Emory University; Peter J. Magill, University of Oxford; Andrew Sharott, University of Oxford
• Language: English
• Date: 2018-04-01
• Publisher: Wiley: 12 months
• Publication Version: Final Published Version
• Copyright Statement: © 2017 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc.
• License: Creative Commons Attribution 4.0 International
• Final Published Version (URL): http://dx.doi.org/10.1002/cne.24373
• Title of Journal or Parent Work: Journal of Comparative Neurology
• ISSN: 0021-9967
• Volume: 526
• Issue: 5
• Start Page: 877
• End Page: 898
• Grant/Funding Information: Y.S. was supported by NIH support to Yerkes National Primate Centre (P51OD011132).; F.V. was supported by an MRC studentship.; R.S. was funded by a Wellcome Trust Clinical Fellowship (WT_RS_109030/Z/15/Z).; F.N.G. and E.K. were supported by University of Oxford Clarendon Fund Scholarships and the MRC.; This work was supported by the Medical Research Council UK (MRC; awards MC_UU_12020/5 and MC_UU_12024/2 to P.J.M., and award MC_UU_12024/1 to A.S.), and a Marie Curie European Re‐integration Grant (SNAP‐PD) awarded by the European Union.
• Keywords: RRID: AB_2228331; RRID: AB_94259; Science & Technology; Life Sciences & Biomedicine; Neurosciences; GABAERGIC INTERNEURONS; BETA-OSCILLATIONS; interneuron; RRID: AB_2064130; CHOLINERGIC INTERNEURONS; RHESUS-MONKEYS; SUBVENTRICULAR ZONE; GLOBUS-PALLIDUS; RRID: AB_10000342; BASAL GANGLIA; neuronal diversity; RRID: AB_2269934; Zoology; CEREBRAL-CORTEX; calretinin; striatum; Neurosciences & Neurology; CALCIUM-BINDING PROTEINS; secretagogin; RRID: AB_10864618; RRID: AB_2194626; SUBTHALAMIC NUCLEUS
• Research Categories: Biology, Zoology; Engineering, Biomedical; Biology, Neuroscience

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 three 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.