Open AccessMesenchymal PGD2 activates an ILC2-Treg axis to promote proliferation of normal and malignant HSPCs
Author(s) -
Limei Wu,
Qiqi Lin,
Zhilin Ma,
Fabliha Ahmed Chowdhury,
Habibul Hasan Mazumder,
Wei Du
Publication year - 2020
Publication title -
leukemia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.539
H-Index - 192
eISSN - 1476-5551
pISSN - 0887-6924
DOI - 10.1038/s41375-020-0843-8
Subject(s) - mesenchymal stem cell , prostaglandin d2 , cancer research , haematopoiesis , progenitor cell , foxp3 , innate lymphoid cell , inflammation , immunology , biology , leukemia , microbiology and biotechnology , stem cell , receptor , innate immune system , immune system , biochemistry
Cyclooxygenase (COX)-dependent production of prostaglandins (PGs) is known to play important roles in tumorigenesis. PGD 2 has recently emerged as a key regulator of tumor- and inflammation-associated functions. Here we show that mesenchymal stromal cells (MSCs) from patients with acute myeloid leukemia (AML) or normal MSCs overexpressing COX2 promote proliferation of co-cultured hematopoietic stem and progenitor cells (HSPCs), which can be prevented by treatment with COX2 knockdown or TM30089, a specific antagonist of the PGD 2 receptor CRTH2. Mechanistically, we demonstrate that PGD 2 -CRTH2 signaling acts directly on type 2 innate lymphoid cells (ILC2s), potentiating their expansion and driving them to produce Interleukin-5 (IL-5) and IL-13. Furthermore, IL-5 but not IL-13 expands CD4 + CD25 + IL5Rα + T regulatory cells (Tregs) and promotes HSPC proliferation. Disruption of the PGD 2 -activated ILC2-Treg axis by specifically blocking the PGD 2 receptor CRTH2 or IL-5 impedes proliferation of normal and malignant HSPCs. Conversely, co-transfer of CD4 + CD25 + IL5Rα + Tregs promotes malignant HSPC proliferation and accelerates leukemia development in xenotransplanted mice. Collectively, these results indicate that the mesenchymal source of PGD 2 promotes proliferation of normal and malignant HSPCs through activation of the ILC2-Treg axis. These findings also suggest that this novel PGD 2 -activated ILC2-Treg axis may be a valuable therapeutic target for cancer and inflammation-associated diseases.