Intersectional expression of <i>Foxp2</i> and Grp identifies cold-activated parabrachial neurons

The parabrachial nucleus (PB) contains many neuronal subpopulations, including a cold-activated subset that relays thermosensory information to the forebrain. Although these neurons are part of the Atoh1-derived PB macropopulation, their precise genetic identity has remained unclear, limiting cell-type-specific investigation of cold-defense circuitry. In this study, we show that this subpopulation is selectively identified by co-expression of Foxp2 and Grp. This intersectional molecular identity suggests a practical strategy for selectively targeting cold-activated PB neurons, enabling cell-type-specific dissection of the circuit mechanisms underlying autonomic and behavioral cold-defense responses.

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Publication Details

Journal
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Published
2026-05-27
DOI
https://doi.org/10.1152/ajpregu.00133.2026
Primary Topic
Neuroscience of respiration and sleep
Type
article
Field-Weighted Citation Impact
0.00

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article

Intersectional expression of Foxp2 and Grp identifies cold-activated parabrachial neurons

Joel C. Geerling, Fillan S. Grady, Silvia Gasparini, Haidong Zhu et al.
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
Neuroscience of respiration and sleep
article

Intersectional expression of Foxp2 and Grp identifies cold-activated parabrachial neurons

Joel C. Geerling, Fillan S. Grady, Silvia Gasparini, Haidong Zhu, Mya L. leaung
article en

Abstract

The parabrachial nucleus (PB) contains many neuronal subpopulations, including a cold-activated subset that relays thermosensory information to the forebrain. Although these neurons are part of the Atoh1-derived PB macropopulation, their precise genetic identity has remained unclear, limiting cell-type-specific investigation of cold-defense circuitry. In this study, we show that this subpopulation is selectively identified by co-expression of Foxp2 and Grp. This intersectional molecular identity suggests a practical strategy for selectively targeting cold-activated PB neurons, enabling cell-type-specific dissection of the circuit mechanisms underlying autonomic and behavioral cold-defense responses.

American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
University of Iowa (US), University of Washington (US)
Roy J. Carver Charitable Trust, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 8%
Neuroscience of respiration and sleep
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