Human fetal membrane expression of IL-19 and IL-20 and its differential effect on inflammatory cytokine production

Ramkumar Menon, Lana Ismail, Deema Ismail, Mario Merialdi, Salvatore J. Lombardi, Stephen J. Fortunato

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Objective. The objectives of this study were to document the expression of IL-19 and IL-20, localize their expression in human fetal membranes and to examine their influence on the production of other inflammatory cytokines (IL-1, IL-6, IL-8, and TNF-α) from placental membranes. Methods. Human fetal membranes collected at term from normal pregnancies were stimulated with either recombinant human IL-19, IL-20, bacterial endotoxin (LPS) alone or the cytokine + LPS. The expression of IL-19 and IL-20 was studied by reverse transcriptase polymerase chain reaction (RT-PCR) and localized using immunohistochemistry. Concentrations of IL-1, IL-6, IL-8, and TNF-α were measured with multiplex sandwich immunoassay using microsphere technology. Results. RT-PCR documented IL-19 and IL-20 gene expression in fetal membranes. Immunohistochemistry localized both peptides to amnion and chorion layers. LPS stimulated the production of all four cytokines (IL-1, IL-6, IL-8, and TNF-α) from fetal membranes compared to unstimulated controls. No change in IL-1 and IL-8 concentration was seen after IL-19 or IL-20 stimulation, whereas IL-6 concentration was three- and two-fold higher after IL-19 and IL-20 treatment, respectively. TNF levels were unchanged after IL-19 and IL-20 treatment; however, TNF levels were significantly decreased in membranes treated with IL-19 or IL-20 + LPS compared to LPS alone. Conclusion. Fetal membranes are a source of IL-19 and IL-20. These cytokines act as an inhibitory agent to LPS-induced TNF production whereas they stimulate IL-6 production and have no effect on IL-1 and IL-8 production from human fetal membranes. The effect of IL-19 and IL-20 in pregnancy will be dependent on their concentrations and other environmental factors such as infection.

Original languageEnglish (US)
Pages (from-to)209-214
Number of pages6
JournalJournal of Maternal-Fetal and Neonatal Medicine
Volume19
Issue number4
DOIs
StatePublished - Apr 2006
Externally publishedYes

Fingerprint

Extraembryonic Membranes
Cytokines
Interleukin-8
Interleukin-1
Interleukin-6
Reverse Transcriptase Polymerase Chain Reaction
Immunohistochemistry
interleukin 20
Chorion
Pregnancy
Amnion
Membranes
Microspheres
Immunoassay
Endotoxins
Technology
Gene Expression

Keywords

  • Amniochorion
  • Cytokines
  • IL-10
  • IL-6
  • Inflammation
  • Term labor
  • TNF-alpha

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology

Cite this

Human fetal membrane expression of IL-19 and IL-20 and its differential effect on inflammatory cytokine production. / Menon, Ramkumar; Ismail, Lana; Ismail, Deema; Merialdi, Mario; Lombardi, Salvatore J.; Fortunato, Stephen J.

In: Journal of Maternal-Fetal and Neonatal Medicine, Vol. 19, No. 4, 04.2006, p. 209-214.

Research output: Contribution to journalArticle

Menon, Ramkumar ; Ismail, Lana ; Ismail, Deema ; Merialdi, Mario ; Lombardi, Salvatore J. ; Fortunato, Stephen J. / Human fetal membrane expression of IL-19 and IL-20 and its differential effect on inflammatory cytokine production. In: Journal of Maternal-Fetal and Neonatal Medicine. 2006 ; Vol. 19, No. 4. pp. 209-214.
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T1 - Human fetal membrane expression of IL-19 and IL-20 and its differential effect on inflammatory cytokine production

AU - Menon, Ramkumar

AU - Ismail, Lana

AU - Ismail, Deema

AU - Merialdi, Mario

AU - Lombardi, Salvatore J.

AU - Fortunato, Stephen J.

PY - 2006/4

Y1 - 2006/4

N2 - Objective. The objectives of this study were to document the expression of IL-19 and IL-20, localize their expression in human fetal membranes and to examine their influence on the production of other inflammatory cytokines (IL-1, IL-6, IL-8, and TNF-α) from placental membranes. Methods. Human fetal membranes collected at term from normal pregnancies were stimulated with either recombinant human IL-19, IL-20, bacterial endotoxin (LPS) alone or the cytokine + LPS. The expression of IL-19 and IL-20 was studied by reverse transcriptase polymerase chain reaction (RT-PCR) and localized using immunohistochemistry. Concentrations of IL-1, IL-6, IL-8, and TNF-α were measured with multiplex sandwich immunoassay using microsphere technology. Results. RT-PCR documented IL-19 and IL-20 gene expression in fetal membranes. Immunohistochemistry localized both peptides to amnion and chorion layers. LPS stimulated the production of all four cytokines (IL-1, IL-6, IL-8, and TNF-α) from fetal membranes compared to unstimulated controls. No change in IL-1 and IL-8 concentration was seen after IL-19 or IL-20 stimulation, whereas IL-6 concentration was three- and two-fold higher after IL-19 and IL-20 treatment, respectively. TNF levels were unchanged after IL-19 and IL-20 treatment; however, TNF levels were significantly decreased in membranes treated with IL-19 or IL-20 + LPS compared to LPS alone. Conclusion. Fetal membranes are a source of IL-19 and IL-20. These cytokines act as an inhibitory agent to LPS-induced TNF production whereas they stimulate IL-6 production and have no effect on IL-1 and IL-8 production from human fetal membranes. The effect of IL-19 and IL-20 in pregnancy will be dependent on their concentrations and other environmental factors such as infection.

AB - Objective. The objectives of this study were to document the expression of IL-19 and IL-20, localize their expression in human fetal membranes and to examine their influence on the production of other inflammatory cytokines (IL-1, IL-6, IL-8, and TNF-α) from placental membranes. Methods. Human fetal membranes collected at term from normal pregnancies were stimulated with either recombinant human IL-19, IL-20, bacterial endotoxin (LPS) alone or the cytokine + LPS. The expression of IL-19 and IL-20 was studied by reverse transcriptase polymerase chain reaction (RT-PCR) and localized using immunohistochemistry. Concentrations of IL-1, IL-6, IL-8, and TNF-α were measured with multiplex sandwich immunoassay using microsphere technology. Results. RT-PCR documented IL-19 and IL-20 gene expression in fetal membranes. Immunohistochemistry localized both peptides to amnion and chorion layers. LPS stimulated the production of all four cytokines (IL-1, IL-6, IL-8, and TNF-α) from fetal membranes compared to unstimulated controls. No change in IL-1 and IL-8 concentration was seen after IL-19 or IL-20 stimulation, whereas IL-6 concentration was three- and two-fold higher after IL-19 and IL-20 treatment, respectively. TNF levels were unchanged after IL-19 and IL-20 treatment; however, TNF levels were significantly decreased in membranes treated with IL-19 or IL-20 + LPS compared to LPS alone. Conclusion. Fetal membranes are a source of IL-19 and IL-20. These cytokines act as an inhibitory agent to LPS-induced TNF production whereas they stimulate IL-6 production and have no effect on IL-1 and IL-8 production from human fetal membranes. The effect of IL-19 and IL-20 in pregnancy will be dependent on their concentrations and other environmental factors such as infection.

KW - Amniochorion

KW - Cytokines

KW - IL-10

KW - IL-6

KW - Inflammation

KW - Term labor

KW - TNF-alpha

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DO - 10.1080/14767050500440986

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