Mapping the adult human esophagus in vivo and in vitro

Author:

Ferrer-Torres Daysha12ORCID,Wu Joshua H.1ORCID,Zhang Charles J.13ORCID,Hammer Max A.1ORCID,Dame Michael K.1ORCID,Wu Angeline1,Holloway Emily M.4,Karpoff Kateryna1,McCarthy Caroline L.1,Bohm Margaret S.1ORCID,Cuttitta Ashley J.1,Tigani Dominic J.1,Huang Sha1,Tsai Yu-Hwai1,Miller Alyssa J.1ORCID,Walker Taylor1,Bayer David E.1,Hogan Simon P.5,Turgeon Danielle Kim1,Lin Jules6,Higgins Peter D. R.1ORCID,Sexton Jonathan137ORCID,Spence Jason R.1482ORCID

Affiliation:

1. University of Michigan Medical School 1 Department of Internal Medicine, Division of Gastroenterology , , Ann Arbor, MI 48109, USA

2. Center for Cell Plasticity and Organ Design, University of Michigan Medical School 2 , Ann Arbor, MI 48109, USA

3. College of Pharmacy, University of Michigan 3 Department of Medicinal Chemistry , , Ann Arbor, MI 48109, USA

4. University of Michigan Medical School 4 Department of Cell and Developmental Biology , , Ann Arbor, MI 48109, USA

5. University of Michigan Medical School 5 Department of Pathology , , Ann Arbor, MI 48109, USA

6. University of Michigan Medical School 6 Department of Thoracic Surgery , , Ann Arbor, MI 48109, USA

7. U-M Center for Drug Repurposing, University of Michigan 7 , Ann Arbor, MI 48109, USA

8. University of Michigan Medical School 8 Department of Biomedical Engineering , , Ann Arbor, MI 48109, USA

Abstract

ABSTRACT Many esophageal diseases can arise during development or throughout life. Therefore, well-characterized in vitro models and detailed methods are essential for studying human esophageal development, homeostasis and disease. Here, we (1) create an atlas of the cell types observed in the normal adult human esophagus; (2) establish an ancestrally diverse biobank of in vitro esophagus tissue to interrogate homeostasis and injury; and (3) benchmark in vitro models using the adult human esophagus atlas. We created a single-cell RNA sequencing reference atlas using fresh adult esophagus biopsies and a continuously expanding biobank of patient-derived in vitro cultures (n=55 lines). We identify and validate several transcriptionally distinct cell classes in the native human adult esophagus, with four populations belonging to the epithelial layer, including basal, epibasal, early differentiating and terminally differentiated luminal cells. Benchmarking in vitro esophagus cultures to the in vivo reference using single-cell RNA sequencing shows that the basal stem cells are robustly maintained in vitro, and the diversity of epithelial cell types in culture is dependent on cell density. We also demonstrate that cultures can be grown in 2D or as 3D organoids, and these methods can be employed for modeling the complete epithelial layers, thereby enabling in vitro modeling of the human adult esophagus.

Funder

Chan Zuckerberg Initiative

University of Michigan Center for Gastrointestinal Research

National Institute of Diabetes and Digestive and Kidney Diseases

Medical School, University of Michigan

Michigan Institute for Clinical and Health Research

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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