Whole-brain mapping of histaminergic projections in mouse brain

Author:

Lin Wenkai12ORCID,Xu Lingyu1,Zheng Yanrong2,An Sile3,Zhao Mengting3ORCID,Hu Weiwei1ORCID,Li Mengyao4,Dong Hui4ORCID,Li Anan5ORCID,Li Yulong4ORCID,Gong Hui5,Pan Gang6,Wang Yi127ORCID,Luo Qingming8,Chen Zhong127ORCID

Affiliation:

1. Institute of Pharmacology and Toxicology, Key Laboratory of Medical Neurobiology of the Ministry of Health of China, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China

2. Key Laboratory of Neuropharmacology and Translational Medicine of Zhejiang Province, School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China

3. Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics, Ministry of Education Key Laboratory for Biomedical Photonics, Huazhong University of Science and Technology, Wuhan 430074, China

4. State Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing 100871, China

5. Huazhong University of Science and Technology-Suzhou Institute for Brainsmatics, Jiangsu Industrial Technology Research Institute for Brainsmatics, Suzhou 215000, China

6. Department of Computer Science, Zhejiang University, Hangzhou 310058, China

7. Epilepsy Center, Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China

8. Key Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University, Haikou 570228, China

Abstract

Histamine is a conserved neuromodulator in mammalian brains and critically involved in many physiological functions. Understanding the precise structure of the histaminergic network is the cornerstone in elucidating its function. Herein, using histidine decarboxylase (HDC)-CreERT2 mice and genetic labeling strategies, we reconstructed a whole-brain three dimensional (3D) structure of histaminergic neurons and their outputs at 0.32 × 0.32 × 2 μm 3 pixel resolution with a cutting-edge fluorescence microoptical sectioning tomography system. We quantified the fluorescence density of all brain areas and found that histaminergic fiber density varied significantly among brain regions. The density of histaminergic fiber was positively correlated with the amount of histamine release induced by optogenetic stimulation or physiological aversive stimulation. Lastly, we reconstructed a fine morphological structure of 60 histaminergic neurons via sparse labeling and uncovered the largely heterogeneous projection pattern of individual histaminergic neurons. Collectively, this study reveals an unprecedented whole-brain quantitative analysis of histaminergic projections at the mesoscopic level, providing a foundation for future functional histaminergic study.

Funder

The National Key R&D Program of China

National Natural Science Foundation of China

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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