Multiplex imaging of murine bone marrow using Phenocycler 2.0™

Bone marrow (BM) is a tissue that is of great importance to several areas of basic and translational research, including hematology, oncology, bone biology, and immunology. It is unique in that it is gelatinous in nature but housed in a hard casing of bone. Traditionally, flow cytometry and immunofluorescence (IF) techniques have been employed to study the composition of cellular interactions and elements of the BM. However, it has been challenging to study the BM in an unperturbed state using multiple fluorescent probes at a time to fully appreciate the diverse cell populations and their interactions and relative positioning with each other. This protocol addresses how Phenocycler 2.0<sup>TM</sup>, which uses co-detection by indexing (CODEX) in conjunction with HALO 4.0<sup>TM</sup> image analysis software, can overcome the obstacles faced by traditional techniques used to study the BM in an unperturbed state.

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Publication Details

Journal
Leukemia
Published
2025-04-11
DOI
https://doi.org/10.1038/s41375-025-02596-5
Citations
1
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.80

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article

Multiplex imaging of murine bone marrow using Phenocycler 2.0™

Connor J. Gulbronson, Izza Khurram, Sonali Karnik, Melissa A. Kacena et al.
1 citations
Leukemia
Immune cells in cancer
0.80
article

Multiplex imaging of murine bone marrow using Phenocycler 2.0™

Connor J. Gulbronson, Izza Khurram, Sonali Karnik, Melissa A. Kacena, Rahul Kanumuri, Reuben Kapur, Baskar Ramdas, Peter Jordan, Melissa Hartman, Karen E. Pollok, Ramesh Kumar, Pratibha Singh, Drew M. Brown
article en
1 citations

Abstract

Bone marrow (BM) is a tissue that is of great importance to several areas of basic and translational research, including hematology, oncology, bone biology, and immunology. It is unique in that it is gelatinous in nature but housed in a hard casing of bone. Traditionally, flow cytometry and immunofluorescence (IF) techniques have been employed to study the composition of cellular interactions and elements of the BM. However, it has been challenging to study the BM in an unperturbed state using multiple fluorescent probes at a time to fully appreciate the diverse cell populations and their interactions and relative positioning with each other. This protocol addresses how Phenocycler 2.0<sup>TM</sup>, which uses co-detection by indexing (CODEX) in conjunction with HALO 4.0<sup>TM</sup> image analysis software, can overcome the obstacles faced by traditional techniques used to study the BM in an unperturbed state.

LeukemiaVol. 39(6)
Indiana University Health (US), University of Indianapolis (US), Richard L. Roudebush VA Medical Center (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US)
National Institutes of Health, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Openalex Percentile: Top 29%
Immune cells in cancer
0.80
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