Mesenchymal stromal cells are non-hematopoietic, multipotent progenitor cells producing cytokines, chemokines, and extracellular matrix proteins that support hematopoietic stem cell survival and engraftment, influence immune effector cell development, maturation, and function, and inhibit alloreactive T-cell responses. The immunosuppressive properties of human mesenchymal stromal cells have attracted much attention from immunologists, stem cell biologists and clinicians. Recently, the presence of the endocannabinoid system in hematopoietic and neural stem cells has been demonstrated. Endocannabinoids, mainly acting through the cannabinoid receptor subtype 2, are able to modulate cytokine release and to act as immunosuppressant when added to activated T lymphocytes. In the present study, we have investigated, through a multidisciplinary approach, the involvement of the endocannabinoids in migration, viability and cytokine release of human mesenchymal stromal cells. We show, for the first time, that cultures of human mesenchymal stromal cells express all of the components of the endocannabinoid system, suggesting a potential role for the cannabinoid CB2 receptor as a mediator of anti-inflammatory properties of human mesenchymal stromal cells, as well as of their survival pathways and their capability to home and migrate towards endocannabinoid sources.

The cannabinoid receptor type 2 as mediator of mesenchymal stromal cell immunosuppressive properties.

LOCATELLI, FRANCO;
2013-01-01

Abstract

Mesenchymal stromal cells are non-hematopoietic, multipotent progenitor cells producing cytokines, chemokines, and extracellular matrix proteins that support hematopoietic stem cell survival and engraftment, influence immune effector cell development, maturation, and function, and inhibit alloreactive T-cell responses. The immunosuppressive properties of human mesenchymal stromal cells have attracted much attention from immunologists, stem cell biologists and clinicians. Recently, the presence of the endocannabinoid system in hematopoietic and neural stem cells has been demonstrated. Endocannabinoids, mainly acting through the cannabinoid receptor subtype 2, are able to modulate cytokine release and to act as immunosuppressant when added to activated T lymphocytes. In the present study, we have investigated, through a multidisciplinary approach, the involvement of the endocannabinoids in migration, viability and cytokine release of human mesenchymal stromal cells. We show, for the first time, that cultures of human mesenchymal stromal cells express all of the components of the endocannabinoid system, suggesting a potential role for the cannabinoid CB2 receptor as a mediator of anti-inflammatory properties of human mesenchymal stromal cells, as well as of their survival pathways and their capability to home and migrate towards endocannabinoid sources.
2013
Immunology incorporates cellular and molecular studies in immunology, as well as clinical research in immunopathology, infectious disease, autoimmunity, and allergy. Host-pathogen interactions in infectious disease, as well as experimental therapeutic applications of immunomodulating agents are also considered. Resources dealing primarily with the biology of microbial, viral, or parasitic pathogens are excluded and are covered in the Microbiology category.
Esperti anonimi
Inglese
Internazionale
8
e80022
Adult, Cell Differentiation, Cell Movement, Cell Survival, Cytokines; metabolism, Endocannabinoids; metabolism, Female, Gene Expression, Humans, Immunomodulation, Inflammation Mediators; metabolism, Male, Mesenchymal Stromal Cells; cytology/immunology/metabolism, Middle Aged, Mitogen-Activated Protein Kinase 1; metabolism, Receptor; Cannabinoid; CB1; genetics/metabolism, Receptor; CB2; agonists/genetics/metabolism, Ribosomal Protein S6 Kinases; 70-kDa; metabolism, Signal Transduction, TOR Serine-Threonine Kinases; metabolism, Young Adult
http://dx.doi.org/10.1371/journal.pone.0080022
14
info:eu-repo/semantics/article
262
F., Rossi; M. E., Bernardo; G., Bellini; L., Luongo; A., Conforti; I., Manzo; F., Guida; L., Cristino; R., Imperatore; S., Petrosino; B., Nobili; V. D...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/992810
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