Gene interactions and pathways from curated databases and text-mining
Invest Ophthalmol Vis Sci 2001, PMID: 11381071

Differential chemokine regulation by Th2 cytokines during human RPE-monocyte coculture.

Yoshida, A; Elner, S G; Bian, Z M; Kunkel, S L; Lukacs, N W; Elner, V M

OBJECTIVE

To determine the effects of the potent anti-inflammatory Th2 cytokines, interleukin (IL)-4, -10, and -13, on IL-8 and monocyte chemoattractant protein (MCP) 1 production by human retinal pigment epithelial (HRPE) cells, monocytes, and HRPE cell-monocyte cocultures.

METHODS

Enzyme-linked immunosorbent assays were performed to determine IL-8 and MCP-1 secretion by HRPE cells, monocytes, and HRPE cell-monocyte cocultures stimulated with IL-1beta or TNF-alpha, either alone, or in combination with IL-4, -10, or -13, at various time points.

RESULTS

IL-4 and -13, but not IL-10, enhanced constitutive and TNF-alpha-induced HRPE IL-8 and MCP-1 secretion. IL-4 also enhanced IL-1beta-induced HRPE IL-8. IL-4 and -13 reduced monocyte IL-8 and MCP-1, whereas IL-10 reduced monocyte IL-8 but enhanced MCP-1. Overlay of monocytes onto HRPE cell cultures resulted in increased IL-8 and MCP-1 secretion. IL-8 secretion by HRPE cell-monocyte cocultures was inhibited by IL-4, -10, and -13, whereas MCP-1 was inhibited only by IL-10. These cytokines also inhibited IL-1beta potentiation of IL-8, but not MCP-1 secretion by cocultures. IL-4 enhanced TNF-alpha potentiation of chemokine secretion by cocultures, whereas IL-10 had no effects. IL-13 potentiated TNF-alpha-induced MCP-1, but not IL-8 secretion by cocultures.

CONCLUSIONS

IL-4, -10 and -13 have complex effects on chemokine secretion by HRPE cells, monocytes, and HRPE cell-monocyte cocultures. IL-10 appears to be the most consistently suppressive cytokine, suggesting potential therapeutic usefulness of IL-10 in the treatment of ocular inflammatory and proliferative diseases.

Document information provided by NCBI PubMed

Text Mining Data

MCP-1 → TNF-alpha: " IL-4 and -13, but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

MCP-1 → IL-10: " IL-4 and -13, but not IL-10 , enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

MCP-1 → IL-4 and -13: " IL-4 and -13 , but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

MCP-1 → IL-4: " IL-4 and -13, but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

IL-8 → TNF-alpha: " IL-4 and -13, but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

IL-8 → IL-10: " IL-4 and -13, but not IL-10 , enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

IL-8 → IL-4 and -13: " IL-4 and -13 , but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

IL-8 → IL-4: " IL-4 and -13, but not IL-10, enhanced constitutive and TNF-alpha induced HRPE IL-8 and MCP-1 secretion "

IL-8 → IL-1beta: " IL-4 also enhanced IL-1beta induced HRPE IL-8 "

IL-8 → IL-4: " IL-4 also enhanced IL-1beta induced HRPE IL-8 "

MCP-1 → IL-10: " IL-4 and -13 reduced monocyte IL-8 and MCP-1, whereas IL-10 reduced monocyte IL-8 but enhanced MCP-1 "

MCP-1 ⊣ IL-10: " IL-8 secretion by HRPE cell-monocyte cocultures was inhibited by IL-4, -10, and -13, whereas MCP-1 was inhibited only by IL-10 "

IL-8 ⊣ IL-4: " IL-8 secretion by HRPE cell-monocyte cocultures was inhibited by IL-4 , -10, and -13, whereas MCP-1 was inhibited only by IL-10 "

MCP-1 → TNF-alpha: " IL-13 potentiated TNF-alpha induced MCP-1 , but not IL-8 secretion by cocultures "

MCP-1 → IL-13: " IL-13 potentiated TNF-alpha induced MCP-1 , but not IL-8 secretion by cocultures "

IL-8 → TNF-alpha: " IL-13 potentiated TNF-alpha induced MCP-1, but not IL-8 secretion by cocultures "

IL-8 → IL-13: " IL-13 potentiated TNF-alpha induced MCP-1, but not IL-8 secretion by cocultures "

Manually curated Databases

No curated data.