The characterization of chemokine production and chemokine receptor expression reveals possible functional cross-talks in AML blasts with monocytic differentiation

Alessandro Cignetti, Antonella Vallario, Ilaria Roato, Paola Circosta, Giuliana Strola, Cristina Scielzo, Bernardino Allione, Lucia Garetto, Federico Caligaris-Cappio, Paolo Ghia

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Abstract

Objective. The mechanisms regulating the trafficking of leukemic myeloid blasts are poorly understood. A differential expression of chemokines and chemokine receptors might account for some aspects of the pattern of invasion and accumulation of leukemic cells. We aimed at defining the pattern of chemokine and chemokine receptor expression of acute myeloid leukemia (AML) blasts in comparison with their putative normal cell counterparts. Patients and Methods. Twenty-five cases of AML were analyzed by flow cytometry for the expression of several chemokine receptors and by RT-PCR for the expression of relevant chemokines. For selected chemokines, the production was confirmed by ELISA. AML blasts were also assessed for their migration capacity in response to autologous supernatants and recombinant chemokines. Results. Undifferentiated AML (MO-M1 and some M2) express only CXCR4 on their surfaceand produce mainly inflammatory chemokines, resembling normal CD34+ progenitors. More differentiated AML (M4-M5 and some M2) have a more diversified receptor repertoire and, besides CXCR4, express the receptors for inflammatory chemokines and produce both constitutive and inflammatory chemokines, resembling resting and activated monocytes. In particular, M4-M5 blasts produce MCP-1 and MIP-3α and also express their specific receptors (CCR2 and, to a lesser extent, CCR6) and migrate in vitro in response to MCP-1 and MIP-3α and to their own supernatant. A significant correlation between extramedullary involve-ment and coexpression of MCP-1/CCR2 was found. Conclusions. These data suggest that chemokines and their receptors segregate within the different FAB subtypes and, by allowing cross-talk among members of the malignant clone, might help to explain some aspects of the pattern of invasion in AML with monocytic differentiation.

Original languageEnglish
Pages (from-to)495-503
Number of pages9
JournalExperimental Hematology
Volume31
Issue number6
DOIs
Publication statusPublished - Jun 1 2003

Fingerprint

Chemokine Receptors
Chemokines
Acute Myeloid Leukemia
CCR2 Receptors
Leukemia, Myelomonocytic, Acute
Leukemia, Monocytic, Acute
CXCR4 Receptors
Monocytes
Flow Cytometry
Clone Cells
Enzyme-Linked Immunosorbent Assay
Polymerase Chain Reaction

ASJC Scopus subject areas

  • Cancer Research
  • Cell Biology
  • Genetics
  • Hematology
  • Oncology
  • Transplantation

Cite this

The characterization of chemokine production and chemokine receptor expression reveals possible functional cross-talks in AML blasts with monocytic differentiation. / Cignetti, Alessandro; Vallario, Antonella; Roato, Ilaria; Circosta, Paola; Strola, Giuliana; Scielzo, Cristina; Allione, Bernardino; Garetto, Lucia; Caligaris-Cappio, Federico; Ghia, Paolo.

In: Experimental Hematology, Vol. 31, No. 6, 01.06.2003, p. 495-503.

Research output: Contribution to journalArticle

Cignetti, Alessandro ; Vallario, Antonella ; Roato, Ilaria ; Circosta, Paola ; Strola, Giuliana ; Scielzo, Cristina ; Allione, Bernardino ; Garetto, Lucia ; Caligaris-Cappio, Federico ; Ghia, Paolo. / The characterization of chemokine production and chemokine receptor expression reveals possible functional cross-talks in AML blasts with monocytic differentiation. In: Experimental Hematology. 2003 ; Vol. 31, No. 6. pp. 495-503.
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abstract = "Objective. The mechanisms regulating the trafficking of leukemic myeloid blasts are poorly understood. A differential expression of chemokines and chemokine receptors might account for some aspects of the pattern of invasion and accumulation of leukemic cells. We aimed at defining the pattern of chemokine and chemokine receptor expression of acute myeloid leukemia (AML) blasts in comparison with their putative normal cell counterparts. Patients and Methods. Twenty-five cases of AML were analyzed by flow cytometry for the expression of several chemokine receptors and by RT-PCR for the expression of relevant chemokines. For selected chemokines, the production was confirmed by ELISA. AML blasts were also assessed for their migration capacity in response to autologous supernatants and recombinant chemokines. Results. Undifferentiated AML (MO-M1 and some M2) express only CXCR4 on their surfaceand produce mainly inflammatory chemokines, resembling normal CD34+ progenitors. More differentiated AML (M4-M5 and some M2) have a more diversified receptor repertoire and, besides CXCR4, express the receptors for inflammatory chemokines and produce both constitutive and inflammatory chemokines, resembling resting and activated monocytes. In particular, M4-M5 blasts produce MCP-1 and MIP-3α and also express their specific receptors (CCR2 and, to a lesser extent, CCR6) and migrate in vitro in response to MCP-1 and MIP-3α and to their own supernatant. A significant correlation between extramedullary involve-ment and coexpression of MCP-1/CCR2 was found. Conclusions. These data suggest that chemokines and their receptors segregate within the different FAB subtypes and, by allowing cross-talk among members of the malignant clone, might help to explain some aspects of the pattern of invasion in AML with monocytic differentiation.",
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T1 - The characterization of chemokine production and chemokine receptor expression reveals possible functional cross-talks in AML blasts with monocytic differentiation

AU - Cignetti, Alessandro

AU - Vallario, Antonella

AU - Roato, Ilaria

AU - Circosta, Paola

AU - Strola, Giuliana

AU - Scielzo, Cristina

AU - Allione, Bernardino

AU - Garetto, Lucia

AU - Caligaris-Cappio, Federico

AU - Ghia, Paolo

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N2 - Objective. The mechanisms regulating the trafficking of leukemic myeloid blasts are poorly understood. A differential expression of chemokines and chemokine receptors might account for some aspects of the pattern of invasion and accumulation of leukemic cells. We aimed at defining the pattern of chemokine and chemokine receptor expression of acute myeloid leukemia (AML) blasts in comparison with their putative normal cell counterparts. Patients and Methods. Twenty-five cases of AML were analyzed by flow cytometry for the expression of several chemokine receptors and by RT-PCR for the expression of relevant chemokines. For selected chemokines, the production was confirmed by ELISA. AML blasts were also assessed for their migration capacity in response to autologous supernatants and recombinant chemokines. Results. Undifferentiated AML (MO-M1 and some M2) express only CXCR4 on their surfaceand produce mainly inflammatory chemokines, resembling normal CD34+ progenitors. More differentiated AML (M4-M5 and some M2) have a more diversified receptor repertoire and, besides CXCR4, express the receptors for inflammatory chemokines and produce both constitutive and inflammatory chemokines, resembling resting and activated monocytes. In particular, M4-M5 blasts produce MCP-1 and MIP-3α and also express their specific receptors (CCR2 and, to a lesser extent, CCR6) and migrate in vitro in response to MCP-1 and MIP-3α and to their own supernatant. A significant correlation between extramedullary involve-ment and coexpression of MCP-1/CCR2 was found. Conclusions. These data suggest that chemokines and their receptors segregate within the different FAB subtypes and, by allowing cross-talk among members of the malignant clone, might help to explain some aspects of the pattern of invasion in AML with monocytic differentiation.

AB - Objective. The mechanisms regulating the trafficking of leukemic myeloid blasts are poorly understood. A differential expression of chemokines and chemokine receptors might account for some aspects of the pattern of invasion and accumulation of leukemic cells. We aimed at defining the pattern of chemokine and chemokine receptor expression of acute myeloid leukemia (AML) blasts in comparison with their putative normal cell counterparts. Patients and Methods. Twenty-five cases of AML were analyzed by flow cytometry for the expression of several chemokine receptors and by RT-PCR for the expression of relevant chemokines. For selected chemokines, the production was confirmed by ELISA. AML blasts were also assessed for their migration capacity in response to autologous supernatants and recombinant chemokines. Results. Undifferentiated AML (MO-M1 and some M2) express only CXCR4 on their surfaceand produce mainly inflammatory chemokines, resembling normal CD34+ progenitors. More differentiated AML (M4-M5 and some M2) have a more diversified receptor repertoire and, besides CXCR4, express the receptors for inflammatory chemokines and produce both constitutive and inflammatory chemokines, resembling resting and activated monocytes. In particular, M4-M5 blasts produce MCP-1 and MIP-3α and also express their specific receptors (CCR2 and, to a lesser extent, CCR6) and migrate in vitro in response to MCP-1 and MIP-3α and to their own supernatant. A significant correlation between extramedullary involve-ment and coexpression of MCP-1/CCR2 was found. Conclusions. These data suggest that chemokines and their receptors segregate within the different FAB subtypes and, by allowing cross-talk among members of the malignant clone, might help to explain some aspects of the pattern of invasion in AML with monocytic differentiation.

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