TY - JOUR
T1 - ATP-Binding Cassette Transporter C4 is a Prostaglandin D2 Exporter in HMC-1 cells
AU - Tanaka, Nobuaki
AU - Kawai, Junya
AU - Hirasawa, Noriyasu
AU - Mano, Nariyasu
AU - Yamaguchi, Hiroaki
N1 - Funding Information:
We are grateful to Dr. Piet Borst (Netherlands Cancer Institute) for critically reading the manuscript. This work was in part supported by Japan Society for the Promotion of Science (JSPS) KAKENHI grant number 25460184 and Towa Foundation for Food Science and Research. We would like to thank Editage (www.editage.jp) for English language editing. NT and JK designed and conducted the experiments, analysed the results and wrote the first draft of the manuscript. NH and HY conceived the study and provided technical assistance. All authors contributed to the writing of the manuscript and reviewed the results and approved the final version of the manuscript.
Funding Information:
We are grateful to Dr. Piet Borst (Netherlands Cancer Institute) for critically reading the manuscript. This work was in part supported by Japan Society for the Promotion of Science ( JSPS ) KAKENHI grant number 25460184 and Towa Foundation for Food Science and Research. We would like to thank Editage ( www.editage.jp ) for English language editing.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/8
Y1 - 2020/8
N2 - ATP-binding cassette transporter C4 (ABCC4) is associated with multidrug resistance and the regulation of cell signalling. Some prostaglandins (PGs), including: PGE2, PGF2α, PGE3, and PGF3α are known substrates of ABCC4, and are released from some types of cells to exert their biological effects. In the present study, we demonstrate that PGD2 is a novel substrate of ABCC4 using a transport assay based on inside-out membrane vesicles prepared from ABCC4-overexpressing cells. Then, we used two types of cell lines with confirmed ABCC4 mRNA and PGD2 release capacity (human mast cell lines HMC-1 cells and human rhabdomyosarcoma cell lines TE671 cells) to evaluate the contribution of ABCC4. The extracellular levels of PGD2 were unchanged following addition of a selective ABCC4 inhibitor in TE671 cells. Pharmacological inhibition and knockdown of ABCC4 significantly reduced the extracellular levels of PGD2 by at least 53% in HMC-1 cells. Moreover, the extracellular levels of PGD2 decreased by at least 20% using the selective ABCC4 inhibitor in the other mast cell line RBL-2H3 cells. Therefore, our results suggest that ABCC4 functions as a PGD2 exporter in HMC-1 cells.
AB - ATP-binding cassette transporter C4 (ABCC4) is associated with multidrug resistance and the regulation of cell signalling. Some prostaglandins (PGs), including: PGE2, PGF2α, PGE3, and PGF3α are known substrates of ABCC4, and are released from some types of cells to exert their biological effects. In the present study, we demonstrate that PGD2 is a novel substrate of ABCC4 using a transport assay based on inside-out membrane vesicles prepared from ABCC4-overexpressing cells. Then, we used two types of cell lines with confirmed ABCC4 mRNA and PGD2 release capacity (human mast cell lines HMC-1 cells and human rhabdomyosarcoma cell lines TE671 cells) to evaluate the contribution of ABCC4. The extracellular levels of PGD2 were unchanged following addition of a selective ABCC4 inhibitor in TE671 cells. Pharmacological inhibition and knockdown of ABCC4 significantly reduced the extracellular levels of PGD2 by at least 53% in HMC-1 cells. Moreover, the extracellular levels of PGD2 decreased by at least 20% using the selective ABCC4 inhibitor in the other mast cell line RBL-2H3 cells. Therefore, our results suggest that ABCC4 functions as a PGD2 exporter in HMC-1 cells.
KW - ATP-binding cassette transporter
KW - Mass spectrometry
KW - Mast cell
KW - Prostaglandin
KW - Transporter
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U2 - 10.1016/j.plefa.2020.102139
DO - 10.1016/j.plefa.2020.102139
M3 - Article
C2 - 32544819
AN - SCOPUS:85086606296
SN - 0952-3278
VL - 159
JO - Prostaglandins Leukotrienes and Essential Fatty Acids
JF - Prostaglandins Leukotrienes and Essential Fatty Acids
M1 - 102139
ER -