TY - JOUR
T1 - A novel method to purify neutrophils enables functional analysis of zebrafish hematopoiesis
AU - Konno, Katsuhiro
AU - Kulkeaw, Kasem
AU - Sasada, Manabu
AU - Nii, Takenobu
AU - Kaneyuki, Ayako
AU - Ishitani, Tohru
AU - Arai, Fumio
AU - Sugiyama, Daisuke
N1 - Funding Information:
We thank Drs. Takaaki Kanemaru and Mami Shigeto for technical support, Dr Elise Lamar for critical reading of the manuscript and Dr Kaori Yasuda for analyzing microarray data. This work was partly performed as part of the Cooperative Research Project Program of the Medical Institute of Bioregulation, Kyushu University and supported by the Translational Research Program, Strategic Promotion for Practical Application of Innovative Medical Technology from Japan Agency for Medical Research and Development, AMED.
Publisher Copyright:
© 2020 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd
PY - 2020/12
Y1 - 2020/12
N2 - Zebrafish is a useful model to study vertebrate hematopoiesis, but lack of antibodies to zebrafish proteins has limited purification of hematopoietic cells. Here, we purified neutrophils from larval and adult zebrafish using the lectin Phaseolus vulgaris erythroagglutinin (PHA-E) and DRAQ5, a DNA-staining fluorescent dye. In adult kidney marrow, we purified neutrophil-like PHA-E4low DRAQ5low cells, which neutrophil-type granules. Specifically, at 96-hr post-fertilization, we sorted large-sized cells from larvae using forward scatter and found that they consisted of PHA-Elow DRAQ5low populations. These cells had myeloperoxidase activity, were Sudan Black B-positive and expressed high levels of neutrophil-specific (csf3r and mpx) mRNAs, all neutrophil characteristics. Using this method, we conducted functional analysis suggesting that zyxin (Zyx) plays a role in neutrophil generation in zebrafish larvae. Overall, PHA-E and DRAQ5-based flow cytometry serves as a tool to purify zebrafish neutrophils.
AB - Zebrafish is a useful model to study vertebrate hematopoiesis, but lack of antibodies to zebrafish proteins has limited purification of hematopoietic cells. Here, we purified neutrophils from larval and adult zebrafish using the lectin Phaseolus vulgaris erythroagglutinin (PHA-E) and DRAQ5, a DNA-staining fluorescent dye. In adult kidney marrow, we purified neutrophil-like PHA-E4low DRAQ5low cells, which neutrophil-type granules. Specifically, at 96-hr post-fertilization, we sorted large-sized cells from larvae using forward scatter and found that they consisted of PHA-Elow DRAQ5low populations. These cells had myeloperoxidase activity, were Sudan Black B-positive and expressed high levels of neutrophil-specific (csf3r and mpx) mRNAs, all neutrophil characteristics. Using this method, we conducted functional analysis suggesting that zyxin (Zyx) plays a role in neutrophil generation in zebrafish larvae. Overall, PHA-E and DRAQ5-based flow cytometry serves as a tool to purify zebrafish neutrophils.
UR - http://www.scopus.com/inward/record.url?scp=85093849800&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85093849800&partnerID=8YFLogxK
U2 - 10.1111/gtc.12810
DO - 10.1111/gtc.12810
M3 - Article
C2 - 33006802
AN - SCOPUS:85093849800
SN - 1356-9597
VL - 25
SP - 770
EP - 781
JO - Genes to Cells
JF - Genes to Cells
IS - 12
ER -