TY - JOUR
T1 - Cannabinoid receptors on peripheral leukocytes from patients with schizophrenia
T2 - Evidence for defective immunomodulatory mechanisms
AU - de Campos-Carli, Salvina Maria
AU - Araújo, Marcio Sobreira
AU - de Oliveira Silveira, Amanda Cardoso
AU - de Rezende, Vitor Bortolo
AU - Rocha, Natalia Pessoa
AU - Ferretjans, Rodrigo
AU - Ribeiro-Santos, Rafael
AU - Teixeira-Carvalho, Andrea
AU - Martins-Filho, Olindo Assis
AU - Berk, Michael
AU - Salgado, João Vinícius
AU - Teixeira, Antonio Lucio
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Objectives to evaluate cannabinoid receptors (CBRs) expression on peripheral immune cells, i.e., blood monocytes, neutrophils, lymphocytes, and NK cells, and their relationship to a wide range of serum cytokine levels in subjects with schizophrenia and controls. Methods A sample of 55 people with chronic schizophrenia and 48 controls were enrolled in the study. The expression of the cannabinoid receptors CB1R and CB2R was evaluated in peripheral blood leukocytes by flow cytometry. Serum levels of cytokines/chemokines were simultaneously analyzed by cytometric bead array. Results We found higher expression of cannabinoid receptors on cells of the innate immune system in subjects with schizophrenia when compared with controls. Serum levels of interleukin-4 (IL-4), IL-6, IL-10, IL-17, interferon (IFN-γ), and (C-X-C motif) ligand 10/interferon gamma-induced protein 10 (CXCL10/IP10) were decreased, while levels of the chemokine (C-C motif) ligand 2/monocyte chemoattractant protein-1 (CCL2/MCP-1) were increased in the schizophrenia group in comparison with controls. Patients with schizophrenia showed simpler correlation network between cytokines and CBRs expression than controls. Conclusion Patients with schizophrenia showed increased CBRs expression in cells of the innate immune system and simpler correlation network between cytokines and CBRs expression when compared with controls. These results suggest a defective endocannabinoid system-mediated immunomodulation in patients with schizophrenia.
AB - Objectives to evaluate cannabinoid receptors (CBRs) expression on peripheral immune cells, i.e., blood monocytes, neutrophils, lymphocytes, and NK cells, and their relationship to a wide range of serum cytokine levels in subjects with schizophrenia and controls. Methods A sample of 55 people with chronic schizophrenia and 48 controls were enrolled in the study. The expression of the cannabinoid receptors CB1R and CB2R was evaluated in peripheral blood leukocytes by flow cytometry. Serum levels of cytokines/chemokines were simultaneously analyzed by cytometric bead array. Results We found higher expression of cannabinoid receptors on cells of the innate immune system in subjects with schizophrenia when compared with controls. Serum levels of interleukin-4 (IL-4), IL-6, IL-10, IL-17, interferon (IFN-γ), and (C-X-C motif) ligand 10/interferon gamma-induced protein 10 (CXCL10/IP10) were decreased, while levels of the chemokine (C-C motif) ligand 2/monocyte chemoattractant protein-1 (CCL2/MCP-1) were increased in the schizophrenia group in comparison with controls. Patients with schizophrenia showed simpler correlation network between cytokines and CBRs expression than controls. Conclusion Patients with schizophrenia showed increased CBRs expression in cells of the innate immune system and simpler correlation network between cytokines and CBRs expression when compared with controls. These results suggest a defective endocannabinoid system-mediated immunomodulation in patients with schizophrenia.
KW - Cannabinoid receptors
KW - Cytokines
KW - Endocannabinoid system
KW - Inflammation
KW - Leukocytes
KW - Schizophrenia
UR - http://www.scopus.com/inward/record.url?scp=85006716751&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85006716751&partnerID=8YFLogxK
U2 - 10.1016/j.jpsychires.2016.12.001
DO - 10.1016/j.jpsychires.2016.12.001
M3 - Article
C2 - 28011441
AN - SCOPUS:85006716751
SN - 0022-3956
VL - 87
SP - 44
EP - 52
JO - Journal of Psychiatric Research
JF - Journal of Psychiatric Research
ER -