A nasal cell atlas reveals heterogeneity of tuft cells and their role in directing olfactory stem cell proliferation

Author:

Ualiyeva Saltanat1ORCID,Lemire Evan2ORCID,Wong Caitlin1ORCID,Perniss Alexander1ORCID,Boyd Amelia A.1ORCID,Avilés Evelyn C.3ORCID,Minichetti Dante G.1ORCID,Maxfield Alice4ORCID,Roditi Rachel4ORCID,Matsumoto Ichiro5ORCID,Wang Xin1ORCID,Deng Wenjiang2,Barrett Nora A.1ORCID,Buchheit Kathleen M.1,Laidlaw Tanya M.1ORCID,Boyce Joshua A.1ORCID,Bankova Lora G.1ORCID,Haber Adam L.2ORCID

Affiliation:

1. Division of Allergy and Clinical Immunology, Jeff and Penny Vinik Center for Allergic Disease Research, Brigham and Women’s Hospital and Department of Medicine, Harvard Medical School, Boston, MA, USA.

2. Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

3. Department of Neurobiology, Harvard Medical School, Boston, MA, USA.

4. Division of Otolaryngology–Head and Neck Surgery, Brigham and Women's Hospital and Department of Otolaryngology–Head and Neck Surgery, Harvard Medical School, Boston, MA, USA.

5. Monell Chemical Senses Center, Philadelphia, PA, USA.

Abstract

The olfactory neuroepithelium serves as a sensory organ for odors and forms part of the nasal mucosal barrier. Olfactory sensory neurons are surrounded and supported by epithelial cells. Among them, microvillous cells (MVCs) are strategically positioned at the apical surface, but their specific functions are enigmatic, and their relationship to the other specialized epithelial cells is unclear. Here, we establish that the family of MVCs comprises tuft cells and ionocytes in both mice and humans. Integrating analysis of the respiratory and olfactory epithelia, we define the distinct receptor expression of TRPM5 + tuft-MVCs compared with Gɑ-gustducin high respiratory tuft cells and characterize a previously undescribed population of glandular DCLK1 + tuft cells. To establish how allergen sensing by tuft-MVCs might direct olfactory mucosal responses, we used an integrated single-cell transcriptional and protein analysis. Inhalation of Alternaria induced mucosal epithelial effector molecules including Chil4 and a distinct pathway leading to proliferation of the quiescent olfactory horizontal basal stem cell (HBC) pool, both triggered in the absence of olfactory apoptosis. Alternaria- and ATP-elicited HBC proliferation was dependent on TRPM5 + tuft-MVCs, identifying these specialized epithelial cells as regulators of olfactory stem cell responses. Together, our data provide high-resolution characterization of nasal tuft cell heterogeneity and identify a function of TRPM5 + tuft-MVCs in directing the olfactory mucosal response to allergens.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine,Immunology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3