Brain atlas for glycoprotein hormone receptors at single-transcript level

Author:

Ryu Vitaly12ORCID,Gumerova Anisa12,Korkmaz Funda12,Kang Seong Su3ORCID,Katsel Pavel4ORCID,Miyashita Sari12,Kannangara Hasni12,Cullen Liam12,Chan Pokman5,Kuo TanChun12ORCID,Padilla Ashley12,Sultana Farhath12,Wizman Soleil A1,Kramskiy Natan1,Zaidi Samir6,Kim Se-Min12,New Maria I7,Rosen Clifford J8,Goosens Ki A14ORCID,Frolinger Tal12,Haroutunian Vahram4,Ye Keqiang9,Lizneva Daria12,Davies Terry F12,Yuen Tony12,Zaidi Mone12ORCID

Affiliation:

1. Center for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai

2. Department of Medicine and of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai

3. Department of Pathology, Emory University School of Medicine

4. Department of Psychiatry, Icahn School of Medicine at Mount Sinai

5. Alamak Biosciences

6. Memorial Sloan Kettering Cancer Center

7. Department of Pediatrics, Icahn School of Medicine at Mount Sinai

8. Maine Medical Center Research Institute

9. Faculty of Life and Health Sciences, and Brain Cognition and Brain Disease Institute, Shenzhen Institute of Advanced technology, Chinese Academy of Sciences

Abstract

There is increasing evidence that anterior pituitary hormones, traditionally thought to have unitary functions in regulating single endocrine targets, act on multiple somatic tissues, such as bone, fat, and liver. There is also emerging evidence for anterior pituitary hormone action on brain receptors in mediating central neural and peripheral somatic functions. Here, we have created the most comprehensive neuroanatomical atlas on the expression of TSHR, LHCGR, and FSHR. We have used RNAscope, a technology that allows the detection of mRNA at single-transcript level, together with protein level validation, to document Tshr expression in 173 and Fshr expression in 353 brain regions, nuclei and subnuclei identified using the Atlas for the Mouse Brain in Stereotaxic Coordinates. We also identified Lhcgr transcripts in 401 brain regions, nuclei and subnuclei. Complementarily, we used ViewRNA, another single-transcript detection technology, to establish the expression of FSHR in human brain samples, where transcripts were co-localized in MALAT1-positive neurons. In addition, we show high expression for all three receptors in the ventricular region—with yet unknown functions. Intriguingly, Tshr and Fshr expression in the ependymal layer of the third ventricle was similar to that of the thyroid follicular cells and testicular Sertoli cells, respectively. In contrast, Fshr was localized to NeuN-positive neurons in the granular layer of the dentate gyrus in murine and human brain—both are Alzheimer’s disease-vulnerable regions. Our atlas thus provides a vital resource for scientists to explore the link between the stimulation or inactivation of brain glycoprotein hormone receptors on somatic function. New actionable pathways for human disease may be unmasked through further studies.

Funder

National Institute on Aging

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of General Medical Sciences

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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