A Spatial Transcriptomics Based Label‐Free Method for Assessment of Human Stem Cell Distribution and Effects in a Mouse Model of Lung Fibrosis

Author:

Park Jeongbin1ORCID,Lee Dongjoo1ORCID,Lee Jae Eun1ORCID,Lee Daeseung1ORCID,Song In Ho23,Park Hyun Soo234,Choi Hongyoon156ORCID,Im Hyung‐Jun13789ORCID

Affiliation:

1. Portrai, Inc. 78‐18, Dongsulla‐gil, Jongno‐gu Seoul 03136 Republic of Korea

2. Department of Nuclear Medicine Seoul National University College of Medicine Seoul National University Bundang Hospital 82 Gumi‐ro, 173 Beon‐gil, Bundang‐gu Seongnam 13620 Republic of Korea

3. Department of Molecular Medicine and Biopharmaceutical Sciences Graduate School of Convergence Science and Technology Seoul National University Seoul 08826 Republic of Korea

4. Molim, Inc. Gwanggyo‐ro 145 Yeongtong‐gu Suwon 16229 Republic of Korea

5. Department of Nuclear Medicine Seoul National University Hospital Seoul 03080 Republic of Korea

6. Department of Nuclear Medicine Seoul National University College of Medicine Seoul 03080 Republic of Korea

7. Department of Applied Bioengineering Graduate School of Convergence Science and Technology Seoul National University Seoul 08826 Republic of Korea

8. Cancer Research Institute Seoul National University Seoul 03080 Republic of Korea

9. Research Institute for Convergence Science Seoul National University Seoul 08826 Republic of Korea

Abstract

AbstractRecently, cell therapy has emerged as a promising treatment option for various disorders. Given the intricate mechanisms of action (MOA) and heterogenous distribution in target tissues inherent to cell therapy, it is necessary to develop more sophisticated, unbiased approaches to evaluate the distribution of administered cells and the molecular changes at a microscopic level. This study introduces a label‐free approach for assessing the tissue distribution of administered human mesenchymal stem cells (hMSCs) and their MOA, leveraging spatially resolved transcriptomics (ST) analysis. The hMSCs are introduced into a mouse model with lung fibrosis, followed by the manipulation of ST to visualize the spatial distribution of hMSCs within the tissue. This is achieved by capitalizing on interspecies transcript differences between humans and mice. Furthermore, the method allowed for the examination of molecular changes associated with the spatial distribution of hMSCs. Therefore, this method has the potential to serve as an effective tool for various cell‐based therapeutic agents.

Funder

National Research Foundation of Korea

Korea Drug Development Fund

Korea Evaluation Institute of Industrial Technology

Publisher

Wiley

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