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Dorsoventral Arrangement of Lateral Hypothalamus Populations in the Mouse Hypothalamus: a Prosomeric Genoarchitectonic Analysis

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Journal Mol Neurobiol
Date 2022 Nov 10
PMID 36357614
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Abstract

The lateral hypothalamus (LH) has a heterogeneous cytoarchitectonic organization that has not been elucidated in detail. In this work, we analyzed within the framework of the prosomeric model the differential expression pattern of 59 molecular markers along the ventrodorsal dimension of the medial forebrain bundle in the mouse, considering basal and alar plate subregions of the LH. We found five basal (LH1-LH5) and four alar (LH6-LH9) molecularly distinct sectors of the LH with neuronal cell groups that correlate in topography with previously postulated alar and basal hypothalamic progenitor domains. Most peptidergic populations were restricted to one of these LH sectors though some may have dispersed into a neighboring sector. For instance, histaminergic Hdc-positive neurons were mostly contained within the basal LH3, Nts (neurotensin)- and Tac2 (tachykinin 2)-expressing cells lie strictly within LH4, Hcrt (hypocretin/orexin)-positive and Pmch (pro-melanin-concentrating hormone)-positive neurons appeared within separate LH5 subdivisions, Pnoc (prepronociceptin)-expressing cells were mainly restricted to LH6, and Sst (somatostatin)-positive cells were identified within the LH7 sector. The alar LH9 sector, a component of the Foxg1-positive telencephalo-opto-hypothalamic border region, selectively contained Satb2-expressing cells. Published studies of rodent LH subdivisions have not described the observed pattern. Our genoarchitectonic map should aid in systematic approaches to elucidate LH connectivity and function.

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References
1.
Croizier S, Cardot J, Brischoux F, Fellmann D, Griffond B, Risold P . The vertebrate diencephalic MCH system: a versatile neuronal population in an evolving brain. Front Neuroendocrinol. 2012; 34(2):65-87. DOI: 10.1016/j.yfrne.2012.10.001. View

2.
Diaz C, Puelles L . Developmental Genes and Malformations in the Hypothalamus. Front Neuroanat. 2020; 14:607111. PMC: 7726113. DOI: 10.3389/fnana.2020.607111. View

3.
Li S, De Lecea L . The hypocretin (orexin) system: from a neural circuitry perspective. Neuropharmacology. 2020; 167:107993. DOI: 10.1016/j.neuropharm.2020.107993. View

4.
Shan L, Dauvilliers Y, Siegel J . Interactions of the histamine and hypocretin systems in CNS disorders. Nat Rev Neurol. 2015; 11(7):401-13. PMC: 8744538. DOI: 10.1038/nrneurol.2015.99. View

5.
Yelin-Bekerman L, Elbaz I, Diber A, Dahary D, Gibbs-Bar L, Alon S . Hypocretin neuron-specific transcriptome profiling identifies the sleep modulator Kcnh4a. Elife. 2015; 4:e08638. PMC: 4718730. DOI: 10.7554/eLife.08638. View