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AnnoSpat annotates cell types and quantifies cellular arrangements from spatial proteomics

Aanchal Mongia, Diane C. Saunders, Yue J. Wang, Marcela Brissova, Alvin C. Powers, Klaus H. Kaestner, Golnaz Vahedi, Ali Naji, Gregory W. Schwartz, Robert B. Faryabi
doi: https://doi.org/10.1101/2023.01.15.524135
Aanchal Mongia
1Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
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Diane C. Saunders
7Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University School of Medicine, Nashville, TN, USA
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Yue J. Wang
3Department of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
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Marcela Brissova
7Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University School of Medicine, Nashville, TN, USA
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Alvin C. Powers
6Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, USA
7Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University School of Medicine, Nashville, TN, USA
8VA Tennessee Valley Healthcare System, Nashville, Tennessee, 37212, USA
10Human Pancreas Analysis Program Consortium
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Klaus H. Kaestner
3Department of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
4Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
5Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
10Human Pancreas Analysis Program Consortium
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Golnaz Vahedi
3Department of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
4Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
5Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
10Human Pancreas Analysis Program Consortium
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Ali Naji
2Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
5Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
10Human Pancreas Analysis Program Consortium
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Gregory W. Schwartz
9Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada
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  • For correspondence: Gregory.Schwartz@uhnresearch.ca faryabi@pennmedicine.upenn.edu
Robert B. Faryabi
1Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
4Epigenetics Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA
10Human Pancreas Analysis Program Consortium
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  • For correspondence: Gregory.Schwartz@uhnresearch.ca faryabi@pennmedicine.upenn.edu
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Abstract

Cellular composition and anatomical organization influence normal and aberrant organ functions. Emerging spatial single-cell proteomic assays such as Image Mass Cytometry (IMC) and Co-Detection by Indexing (CODEX) have facilitated the study of cellular composition and organization by enabling high-throughput measurement of cells and their localization directly in intact tissues. However, annotation of cell types and quantification of their relative localization in tissues remain challenging. To address these unmet needs, we developed AnnoSpat (Annotator and Spatial Pattern Finder) that uses neural network and point process algorithms to automatically identify cell types and quantify cell-cell proximity relationships. Our study of data from IMC and CODEX show the superior performance of AnnoSpat in rapid and accurate annotation of cell types compared to alternative approaches. Moreover, the application of AnnoSpat to type 1 diabetic, non-diabetic autoantibody-positive, and non-diabetic organ donor cohorts recapitulated known islet pathobiology and showed differential dynamics of pancreatic polypeptide (PP) cell abundance and CD8+ T cells infiltration in islets during type 1 diabetes progression.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/faryabiLab/AnnoSpat

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted January 18, 2023.
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AnnoSpat annotates cell types and quantifies cellular arrangements from spatial proteomics
Aanchal Mongia, Diane C. Saunders, Yue J. Wang, Marcela Brissova, Alvin C. Powers, Klaus H. Kaestner, Golnaz Vahedi, Ali Naji, Gregory W. Schwartz, Robert B. Faryabi
bioRxiv 2023.01.15.524135; doi: https://doi.org/10.1101/2023.01.15.524135
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AnnoSpat annotates cell types and quantifies cellular arrangements from spatial proteomics
Aanchal Mongia, Diane C. Saunders, Yue J. Wang, Marcela Brissova, Alvin C. Powers, Klaus H. Kaestner, Golnaz Vahedi, Ali Naji, Gregory W. Schwartz, Robert B. Faryabi
bioRxiv 2023.01.15.524135; doi: https://doi.org/10.1101/2023.01.15.524135

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