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In This Article

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

Summary

Transgenic lck:eGFP zebrafish express GFP highly in T lymphocytes, and have been used to study T cell development and acute lymphoblastic leukemia. This line can be used to study B cells, which express lck at lower levels. This protocol describes purification of malignant and non-malignant B cells from lck:eGFP zebrafish.

Abstract

Zebrafish (Danio rerio) are a powerful model to study lymphocyte development. Like mammals, D. rerio possess an adaptive immune system that includes B and T lymphocytes. Studies of zebrafish lymphopoiesis are difficult because antibodies recognizing D. rerio cell surface markers are generally not available, complicating isolation and characterization of different lymphocyte populations, including B-lineage cells. Transgenic lines with lineage-specific fluorophore expression are often used to circumvent this challenge. The transgenic lck:eGFP line has been used to study D. rerio T cell development, and has also been utilized to model T cell development and acute lymphoblastic leukemia (T-ALL). Although lck:eGFP fish have been widely used to analyze the T-lineage, they have not been used to study B cells. Recently, we discovered that many zebrafish B cells also express lck, albeit at lower levels. Consequently, lck:eGFP B cells likewise express low levels of GFP. Based on this finding, we developed a protocol to purify B-lineage cells from lck:eGFP zebrafish, which we report here. Our method describes how to utilize a fluorescent-activated cell sorter (FACS) to purify B cells from lck:eGFP fish or related lines, such as double-transgenic rag2:hMYC; lck:eGFP fish. In these lines, B cells, particularly immature B cells, express GFP at low but detectable levels, allowing them to be distinguished from T cells, which express GFP highly. B cells can be isolated from marrow, thymus, spleen, blood, or other tissues. This protocol provides a new method to purify D. rerio B cells, enabling studies focused on topics like B cell development and B lymphocyte malignancies.

Introduction

Zebrafish offer powerful attributes, such as genetic manipulability, high fecundity, optical translucency, and rapid development that facilitate studying vertebrate development using genetic approaches. These advantages, together with the shared features of teleost and mammalian hematopoiesis, make D. rerio ideal for in vivo analyses of lymphopoiesis and lymphocyte function, from their earliest appearance in larvae throughout adulthood. Blood development in zebrafish relies upon well-conserved genetic processes that are shared with mammals, and these extend to the adaptive immune system. Additionally, molecular mechanisms governing lymphoid development are re....

Protocol

All procedures involving zebrafish were approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Oklahoma Health Sciences Center.

1. Isolating Non-malignant B and T Lymphocytes from Transgenic lck:eGFP Fish

  1. Anesthetize the fish using 0.02% tricaine (MS-222) in fish system water.
  2. Examine 2–6 month old fish for fluorescent thymi, which are located at the dorsomedial aspect of the branchial cavity of zebrafish a.......

Representative Results

We used flow cytometry to analyze and FACS to isolate GFPlo and GFPhi cells from thymus, kidney marrow, and spleen of lck:eGFP transgenic zebrafish. Analysis of 3-month-old fish revealed the thymus contained mostly GFP+ lymphocytes. GFP+ cells were largely confined to the lymphoid gate previously described by Traver et al.17. Two distinct GFP+ populations, GFPloand GFPhi,can<.......

Discussion

We developed and provide a protocol to isolate B cells from lck:eGFP transgenic zebrafish, adding this to other D. rerio models with B-lineage labels3,4. Somewhat surprisingly, the identification of GFPlo B cells in this line went unnoticed since its description in 2004.Generally, lck is considered to be T cell-specific6, but recent studies found unexpected lck expression by natural killer and.......

Acknowledgements

We would like to thank Megan Malone-Perez for zebrafish care, and the OUHSC flow cytometry core. This work was supported by grants from Hyundai Hope on Wheels, the Oklahoma Center for the Advancement of Science and Technology (HRP-067), an NIH/NIGMS INBRE pilot project award (P20 GM103447). JKF holds the E.L. & Thelma Gaylord Endowed Chair in Pediatric Hematology-Oncology of the Children's Hospital Foundation.

....

Materials

NameCompanyCatalog NumberComments
35 µm meshSefar Filter technology7050-1220-000-13
5 ml Polystyrene round-Bottom tube with cell-strainer capFalcon Corning Brand352235
50 ml conical tubeVWR international525-0448
AZ APO 100 Fluorescent microscopeNikon
CytoflexBeckman Coulter
DS-Qi1MC camaraNikon
Ethyl 3-aminobenzoate methansesulfonate; MS-222SigmaE-10521
FACSJazzBD Biosciences
Fetal bovine SerumThermo Fisher10437028
FlowJo v10.2FlowJo, LLC
lck:eGFPSee Langeneu et al., 2004
NIS Elements softwareNikonVersion 4.13
Penicilin -StreptomycinSigmaP4333
Pestle micro-tube homogenizersElectron Microscopy Sciences64788-20
Plastic Transfer pippetes
rag2:hMYC-ERSee Gutierrez et al., 2011
RPMI Media 1640 1XLife Technologies11835-030

References

  1. Paik, E. J., Zon, L. I. Hematopoietic development in the zebrafish. International Journal of Developmental Biology. 54 (6-7), 1127-1137 (2010).
  2. Kasheta, M., et al. Identification and characterization of T reg-like cells in zebrafish.

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B CellsT CellsLCK GFP ZebrafishB ALLT ALLAdaptive Immune SystemMalignanciesFluorescence MicroscopyCell IsolationTissue HomogenizationCell FiltrationPre leukemic FishTumor Categorization

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