TY - JOUR
T1 - Granulocyte macrophage colony-stimulating factor expression in human herpetic stromal keratitis
T2 - implications for the role of neutrophils in HSK
AU - Duan, Rui
AU - Remeijer, Lies
AU - van Dun, Jessica M
AU - Osterhaus, Albert D M E
AU - Verjans, Georges M G M
PY - 2007/1
Y1 - 2007/1
N2 - PURPOSE: Granulocyte macrophage colony-stimulating factor (GM-CSF) is thought to play a key role in chronic inflammatory diseases by governing the survival and function of infiltrating neutrophils. The objective of this study was to determine the putative role of GM-CSF in the pathogenesis of human herpetic stromal keratitis (HSK).METHODS: Primary human corneal fibroblast (HCF) cultures and a telomerase-immortalized human corneal epithelial (HCE) cell line representative of native HCE were stimulated with the known HSK-inducing cytokines interferon (IFN)-gamma, interleukin (IL)-1beta, and tumor necrosis factor (TNF)-alpha. Alternatively, the T-cell cytokine IL-17 was added solely or simultaneously. Human neutrophils were incubated with conditioned medium (CM) of the HCF and HCE stimulated with the aforementioned cytokines, or recombinant GM-CSF, and their viability or activation status was determined by flow cytometry. GM-CSF and IL-8 secretion levels in the CM were determined by ELISA. The antibody-dependent cellular cytotoxicity (ADCC) of neutrophils toward herpes simplex virus (HSV)-infected HCFs was determined by flow cytometry. The expression of GM-CSF was determined in HSK and control corneal buttons by real-time RT-PCR and immunohistology.RESULTS: Compared with IFN-gamma, CM of either cell type stimulated with IL-1beta, or in the case of HCE cells, stimulated with TNF-alpha or IL-17, delayed neutrophil apoptosis significantly. Only in HCFs did IL-17 exhibit a synergistic effect with TNF-alpha. The antiapoptotic activity was attributable in part to the GM-CSF secreted by the activated HCFs and HCE cells. GM-CSF stimulation of neutrophils induced their activation and the secretion of IL-8. GM-CSF did not increase significantly the ADCC reaction of neutrophils toward HSV-infected HCFs. Finally, GM-CSF was expressed in corneas of the patients with HSK but not in control subjects.CONCLUSIONS: The data suggest that GM-CSF, expressed by cornea-resident cells such as HCFs and HCE cells, may play a role in the immunopathogenesis of HSK by prolonging the survival and modulating the effector function of corneal infiltrating neutrophils.
AB - PURPOSE: Granulocyte macrophage colony-stimulating factor (GM-CSF) is thought to play a key role in chronic inflammatory diseases by governing the survival and function of infiltrating neutrophils. The objective of this study was to determine the putative role of GM-CSF in the pathogenesis of human herpetic stromal keratitis (HSK).METHODS: Primary human corneal fibroblast (HCF) cultures and a telomerase-immortalized human corneal epithelial (HCE) cell line representative of native HCE were stimulated with the known HSK-inducing cytokines interferon (IFN)-gamma, interleukin (IL)-1beta, and tumor necrosis factor (TNF)-alpha. Alternatively, the T-cell cytokine IL-17 was added solely or simultaneously. Human neutrophils were incubated with conditioned medium (CM) of the HCF and HCE stimulated with the aforementioned cytokines, or recombinant GM-CSF, and their viability or activation status was determined by flow cytometry. GM-CSF and IL-8 secretion levels in the CM were determined by ELISA. The antibody-dependent cellular cytotoxicity (ADCC) of neutrophils toward herpes simplex virus (HSV)-infected HCFs was determined by flow cytometry. The expression of GM-CSF was determined in HSK and control corneal buttons by real-time RT-PCR and immunohistology.RESULTS: Compared with IFN-gamma, CM of either cell type stimulated with IL-1beta, or in the case of HCE cells, stimulated with TNF-alpha or IL-17, delayed neutrophil apoptosis significantly. Only in HCFs did IL-17 exhibit a synergistic effect with TNF-alpha. The antiapoptotic activity was attributable in part to the GM-CSF secreted by the activated HCFs and HCE cells. GM-CSF stimulation of neutrophils induced their activation and the secretion of IL-8. GM-CSF did not increase significantly the ADCC reaction of neutrophils toward HSV-infected HCFs. Finally, GM-CSF was expressed in corneas of the patients with HSK but not in control subjects.CONCLUSIONS: The data suggest that GM-CSF, expressed by cornea-resident cells such as HCFs and HCE cells, may play a role in the immunopathogenesis of HSK by prolonging the survival and modulating the effector function of corneal infiltrating neutrophils.
KW - Antibody-Dependent Cell Cytotoxicity
KW - Cells, Cultured
KW - Corneal Stroma/cytology
KW - Dose-Response Relationship, Drug
KW - Enzyme-Linked Immunosorbent Assay
KW - Epithelium, Corneal/drug effects
KW - Fibroblasts/drug effects
KW - Granulocyte-Macrophage Colony-Stimulating Factor/genetics
KW - Herpesvirus 1, Human/physiology
KW - Humans
KW - Immunoenzyme Techniques
KW - Interferon-gamma/pharmacology
KW - Interleukin-1beta/pharmacology
KW - Interleukin-8/metabolism
KW - Keratitis, Herpetic/metabolism
KW - Neutrophil Activation
KW - Neutrophils/physiology
KW - RNA/isolation & purification
KW - RNA, Messenger/metabolism
KW - Reverse Transcriptase Polymerase Chain Reaction
KW - Tumor Necrosis Factor-alpha/pharmacology
U2 - 10.1167/iovs.06-0053
DO - 10.1167/iovs.06-0053
M3 - Article
C2 - 17197544
SN - 0146-0404
VL - 48
SP - 277
EP - 284
JO - Investigative ophthalmology & visual science
JF - Investigative ophthalmology & visual science
IS - 1
ER -