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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This experimental protocol describes and optimizes a multiplex immunohistochemistry (IHC) staining method, mainly by optimizing single-channel antibody incubation conditions and adjusting the settings of antibodies and channels to solve the problems of autofluorescence and channel crosstalk in lung cancer tissues of clinical origin.

Abstract

Lung cancer is the leading cause of malignant tumor-related morbidity and mortality all over the world, and the complex tumor microenvironment has been considered the leading cause of death in lung cancer patients. The complexity of the tumor microenvironment requires effective methods to understand cell-to-cell relationships in tumor tissues. The multiplex immunohistochemistry (mIHC) technique has become a key tool for inferring the relationship between the expression of proteins upstream and downstream of signaling pathways in tumor tissues and developing clinical diagnoses and treatment plans. mIHC is a multi-label immunofluorescence staining method based on Tyramine Signal Amplification (TSA) technology, which can simultaneously detect multiple target molecules on the same tissue section sample to achieve different protein co-expression and co-localization analysis. In this experimental protocol, paraffin-embedded tissue sections of lung squamous carcinoma of clinical origin were subjected to multiplex immunohistochemical staining. By optimizing the experimental protocol, multiplex immunohistochemical staining of labeled target cells and proteins was achieved, solving the problem of autofluorescence and channel crosstalk in lung tissues. In addition, multiplex immunohistochemical staining is widely used in the experimental validation of tumor-related, high-throughput sequencing, including single-cell sequencing, proteomics, and tissue space sequencing, providing intuitive and visual pathology validation results.

Introduction

Tyramine signal amplification (TSA), which has a history of more than 20 years, is a class of assay techniques that use horseradish peroxidase (HRP) for high-density in situ labeling of target antigens and is widely applied in enzyme-linked immunosorbent assays (ELISAs), in situ hybridization (ISH), immunohistochemistry (IHC), and other techniques for the detection of biological antigens, substantially improving the sensitivity of the detected signal1. Opal polychromatic staining based on TSA technology has been recently developed and widely used in several studies2,3<....

Protocol

The protocol is approved by the guidelines of the Ethics Committee of West China Hospital, Sichuan University, China. The lung cancer tissue samples were obtained during surgery in the Center of Lung Cancer at West China Hospital, and informed consent was obtained from each patient.

1. Tissue section preparation

  1. FFPE preparation
    1. Immerse clinical tissues in neutral formalin solution for more than 72 h.
    2. Complete the process of dehydrating the t.......

Representative Results

We optimized the matching scheme of CD8 primary antibody and fluorophores. Both sets of fluorescence results corresponded to exactly the same antibody incubation conditions in the experimental group, except for the change in the antibody-matched fluorophore. As shown in Figure 2, there was a significant difference in the channel matching of CD8+ T cells with fluorophore 480 and fluorophore 690. The channel with fluorophore 690 shows an extremely strong fluorescent background-the large area o.......

Discussion

mIHC is an indispensable experimental technique in the field of scientific research for the quantitative and spatial analysis of multiple protein markers at the single-cell level in a single tissue section, providing intuitive and accurate data for the study of disease pathology by focusing on the detailed tissue structure and cellular interactions in the context of the original tissue. The widespread adoption of mIHC technology will require optimized and effective experimental protocols. To address the problems that may.......

Acknowledgements

The authors would like to acknowledge members of the Clinical Pathology Research Institute West China Hospital, who contributed technical guidance for quality multiplex immunofluorescence and IHC processing. This protocol was supported by the National Natural Science Foundation of China (82200078).

....

Materials

NameCompanyCatalog NumberComments
Reagents
Anti-CD8Abcamab237709Primary antibody, 1/100, PH9
Anti-CD68Abcamab955Primary antibody, 1/300, PH9
Anti-CK5/6MilliporeMAB1620Primary antibody, 1/150, PH9
Anti-HMGCS1GeneTexGTX112346Primary antibody, 1/300, PH6
Animal nonimmune serumMXB BiotechnologiesSP KIT-B3Antigen blocking
Fluormount-GSouthernBiotech0100-01Anti-fluorescent burst
Opal PolarisTM 7-Color Manual IHC KitAkoyaNEL861001KTOpal mIHC Staining
Wash BufferDakoK8000/K8002/K8007/K8023Washing the tissues slides
Software
HALOintelligent quantitative tissue analysis software, paid software
inFormintelligent quantitative tissue analysis software, paid software
PerkinElmer Vectramultispectral tissue imaging systems, fully automatic scanning of tissue slides.
QuPath 0.3.2intelligent quantitative tissue analysis software, open source software, used in this experiment.

References

  1. Zaidi, A. U., Enomoto, H., Milbrandt, J., Roth, K. A. Dual fluorescent in situ hybridization and immunohistochemical detection with tyramide signal amplification. The Journal of Histochemistry and Cytochemistry. 48 (10), 1369-1375 (2000).
  2. Lovisa, S., et al.

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Multiplex ImmunohistochemistryMIHCParaffin embeddedLung CancerTissueAutofluorescenceChannel CrosstalkTyramine Signal AmplificationTSACo expressionCo localizationTumor MicroenvironmentHigh throughput SequencingSingle cell SequencingProteomicsTissue Space Sequencing

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