CXCR7 participates in CXCL12-mediated migration and homing of leukemic and normal hematopoietic cells
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CXCR4 was the first receptor identified for CXCL12, but a second receptor, CXCR7, has also been described and its function in hematopoietic cells remains unknown. By inhibition of CXCR4 and/or CXCR7, we showed that CXCR7 participates in normal CD34+ and U937 cell migration and prevents downregulation of CXCR4 by CXCL12 stimulation. In addition, CXCR7 contributes to homing of acute myeloid leukemia and normal progenitor cells to the bone marrow and spleen of NOD/SCID mice. In summary, this study shows an essential role of CXCR7, together with CXCR4, in the control of normal and malignant hematopoietic cell migration and homing induced by CXCL12.
KeywordsCXCR7 Cell migration Homing Hematopoiesis Leukemia
Atypical chemokine receptor 3
Acute myeloid leukemia
Carboxyfluorescein succinimidyl ester
C-X-C motif chemokine ligand 12
C-X-C chemokine receptor type 4
C-X-C chemokine receptor type 7
NOD.CB17-Prkdc scid /J
Short hairpin RNA
CXCR4 was the first receptor identified for CXCL12 , but a second receptor, CXCR7, has also been described . CXCR7 participation in cell migration has been described mainly for malignant solid tumor cells , while the function of CXCR7 in hematopoietic cells remains unknown. Here we investigated the participation of CXCR7 in acute myeloid and normal progenitor cell migration through in vitro assays of chemotaxis induced by CXCL12 and homing in NOD/SCID mice.
Results and discussion
After CXCR7 silencing (lentivirus-mediated shRNA) in U937 cells, a 63% reduction in mRNA and protein levels was verified (data not shown). CXCR7 silencing did not affect the expression of CXCR4 mRNA or protein (data not shown). CXCR4 was silenced by monoclonal antibody blocking, a strategy shown to be largely effective. In normal CD34+ cells, both receptors were blocked with monoclonal antibodies.
The role of both receptors in the migration of U937 and normal CD34+ cells was observed by performing transwell-chemotactic assays, revealing a significant reduction in shCXCR7 U937 cell migration compared to shControl U937 cells (p < 0.001). CXCR4 blocking by mAb also reduced cell migration (p < 0.001). Moreover, CXCR7 silencing plus CXCR4 mAb treatment further inhibited cell chemotactic capacity (p < 0.001; Fig. 1f). Reduction in migration was also observed for normal CD34+ cells with blocked CXCR7 (p < 0.05) or CXCR4 (p < 0.05) or both receptors together (p < 0.01) (Fig. 1g), thus suggesting that CXCR7 contributes to migration towards CXCL12. Previous data, concurring with our results, showed the importance of this receptor in migration of T-cell acute leukemia  as well as AML cell lines HL60, THP-1, and U937 . Kim et al.  performed an in vitro assay, allowing migration of U937 cells, inhibited for CXCR7, against a gradient of CXCL12 and found no significant differences compared to control cells; however, this divergent result may be explained by the short migration time (4 vs 16 h) used in their experiment. Comparing our results to those of Kim’s group, a migration of 16 h evidently led to a more pronounced and suitable result and we are thusconfident that CXCR7, together with CXCR4, controls migration of acute myeloid cells. In addition to migration, we showed that CXCR7 contributes to homing AML and progenitor cells to the bone marrow and spleen, corroborating other studies . Confirming the results of Kim et al, CXCR7inhibition did not modify proliferation or apoptosis of U937 and CD34+ cells (data not shown).
We next examined the influence of CXCR7 on downregulation of CXCR4 in U937 cells induced by CXCL12. Blots were reacted with anti-CXCR4 antibody UMB-2, which recognizes the non-phosphorylated C-terminal epitope 343-352, which undergoes S346/347-phosphorylation upon CXCL12 stimulation. Thus, UMB-2 detects inactive CXCR4 in non-dephosphorylated and total CXCR4 in dephosphorylated samples. Lysate from shControl U937, induced by CXCL12, showed a difference between non-dephosphorylated and dephosphorylated aliquots, characteristic of CXCR4 activation (Fig. 1h, first and second lanes). However, shCXCR7 U937 showed a total CXCR4 decrease when compared with shControl U937 cells (Fig. 1h, third and fourth lanes), suggesting that CXCR7 is important to prevent CXCR4 downregulation in leukemia cells. Thus, we conclude that CXCR7 prevents downregulation of CXCR4 by CXCL12 stimulation.
The biologic function of CXCR7 depends on tissue and organ gene expression. CXCR7 does not activate signals depending on the cell type, only mediating CXCL12 internalization and degradation, acting as a scavenger receptor in cells that signal exclusively through CXCR4 . In other cells, these effects are due to CXCR4 and CXCR7, but through different signaling cascades . Each receiver and different signaling pathway may result in a different effect. Finally, CXCR4 and CXCR7 may form heterodimers, modulating functions mediated through CXCL12/CXCR4 interaction . We further observed that CXCR7 inhibition downregulated CXCR4 expression in AML cells, probably due to excess CXCL12 not scavenged by CXCR7 . Therefore, CXCR7 may be involved in CXCL12 regulation affecting processes mediated by the CXCL12/CXCR4 axis in AML cells. These findings might be extended to normal progenitor cells. Hartmann et al.  described two pools of CXCR7 in CD34+ cells: in the first, CXCR7 was expressed on the cell surface; in the second, the expression was intracellular and associated with early endosomes, which are known to participate in CXCL12 degradation. Hartmann et al. observed that CXCR7 interfered in the ability of CXCR4 to trigger optimal CXCL12-mediated stimulation of integrin activation  and, as observed here, CXCR7 interfered in chemotaxis and homing of CD34+ cells. In summary, this study shows an essential role of CXCR7, together with CXCR4, in controlling normal and malignant hematopoietic cell migration and homing induced by CXCL12.
The authors would like to thank Raquel Susana Foglio for the English review and Tereza Sueko Ide Salles for her invaluable technical assistance.
This study was funded by grants from Fundação de Amparo Pesquisa à do Estado de São Paulo (FAPESP). The authors also thank CNPq, CAPES, and INCT-Sangue for financial support.
Availability of data and materials
Data and material are available by request to the corresponding author.
Conceived and designed the experiments: RCCM and STOS. Performed the experiments: RCCM, KPVF, and STOS. Analyzed the data: RCCM and STOS. Contributed reagents/materials/analysis tools: RCCM, ASSD, and STOS. Wrote the paper: RCCM and STOS. Helped to perform CD34+ separation: ASSD. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Umbilical cord blood samples were obtained from full-term deliveries at the Obstetrics and Gynecology Department, University of Campinas. The study was approved by the Ethics Committee of the University of Campinas and all pregnant women signed informed consent forms.
This study was carried out in strict accordance with the recommendations in the Guide of Care and Use of Laboratory Animals of the University of Campinas Animal Care and used Committee guidelines—CEUA/UNICAMP. The protocol was approved by the Committee on the Ethics of Animal Experiments of the University of Campinas (permit number 2679-1).
Consent for publication
The study was approved by the Ethics Committee of the University of Campinas and all pregnant women signed informed consent forms.
The authors declare that they have no competing interests.
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