Identification and Quantitation of Leukocyte Populations in Human Kidney Tissue by Multi-parameter Flow Cytometry

被引:2
|
作者
Kildey, Katrina [1 ,2 ]
Law, Becker M. P. [1 ,2 ,3 ]
Muczynski, Kimberly A. [4 ]
Wilkinson, Ray [1 ,2 ,3 ,5 ]
Healy, Helen [1 ,2 ,5 ]
Kassianos, Andrew J. [1 ,2 ,3 ,5 ]
机构
[1] Pathol Queensland, Conjoint Kidney Res Lab, Brisbane, Qld, Australia
[2] Royal Brisbane & Womens Hosp, Kidney Hlth Serv, Brisbane, Qld, Australia
[3] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld, Australia
[4] Univ Washington, Div Nephrol, Seattle, WA USA
[5] Univ Queensland, Med Sch, Brisbane, Qld, Australia
来源
BIO-PROTOCOL | 2018年 / 8卷 / 16期
基金
英国医学研究理事会;
关键词
Leukocytes; Kidney; Flow cytometry; Kidney biopsy; Immunology;
D O I
10.21769/BioProtoc.2980
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inflammatory immune cells play direct pathological roles in cases of acute kidney injury (AKI) and chronic kidney disease (CKD). However, the identification and characterization of distinct populations of leukocytes in human kidney biopsies have been confounded by the limitations of immunohistochemical (IHC)-based techniques used to detect them. This methodology is not amenable to the combinations of multiple markers necessary to unequivocally define discrete immune cell populations. We have developed a multi-parameter, flow cytometric-based approach that addresses the need for panels of cell-specific markers in the identification of immune cell populations, allowing both the accurate detection and quantitation of leukocyte subpopulations from a single, clinical kidney biopsy specimen. In this approach, fresh human kidney tissue is dissociated into a single cell suspension followed by antibody-labeling and flow cytometric-based acquisition and analysis. This novel technique provides a major step forward in identifying and enumerating immune cell subpopulations in human kidney disease and is a powerful platform to complement traditional histopathological examinations of clinical kidney biopsies.
引用
收藏
页数:13
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