Herpes simplex virus type 1 alters transcript levels of tumor necrosis factor-α and interleukin-6 in retinal glial cells

Kristen M. Drescher, Judith A. Whittum-Hudson

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Purpose. Studies were performed to determine whether retinal Muller cells transcribe genes for the proinflammatory cytokines interleukin-6 (IL- 6) and tumor necrosis factor-α (TNFα). Isolated murine retinas were used to test whether these cytokines were upregulated in the retina in vivo after anterior chamber inoculation of herpes simplex virus type 1 (HSV-1). The effects of exposure to HSV-1 or interferon-γ (IFNγ) on transcript levels of these cytokines in cultured retinal glia also were examined. Methods. In situ hybridization (ISH) using digoxigenin (DIG)-labeled RNA probes was used to localize mRNA for IL-6 and TNFα in cultured retinal glial cells. Changes in IL-6 and TNFα relative transcript levels were assessed in cultured retinal glial cells using a semiquantitative approach comprised of reverse transcription-polymerase chain reaction (RT-PCR) assay at low amplification cycle number followed by slot blotting and hybridization with DIG-labeled internal sequence probes. In the murine model of herpetic retinitis, the same methods were used to compare temporal changes in relative cytokine transcript levels in retinas isolated from eyes 1 to 7 days after anterior chamber injection of live HSV-1 (KOS strain; 2 x 104 pfu/eye) or buffer with levels in retinas isolated from normal, uninjected eyes. Densitometry was used to quantify relative signal changes obtained with serial diluted samples in slot blot assays. Cytokine signal was normalized to hypoxanthine phosphoribosyl transferase signal obtained from the same cDNA samples. Results. Under baseline culture conditions, ISH and RT-PCR indicated that both IL-6 and TNFα were transcribed by cultured retinal glia. In vitro exposure to either viral (HSV-1) or inflammatory (IFNγ) stimulants increased levels of these transcripts in a time-dependent manner. Peak TNFα mRNA levels were detected 4 hours after exposure to HSV, whereas IL-6 peaked 4 hours later (increases of 10.3 and 8.7 times over baseline, respectively). Differential increases in TNFα and IL-6 transcript levels were detected in retinas isolated from BALB/c mice that received anterior chamber injections of either HSV-1 or Hanks' balanced salt solution (HBSS). By day 3 after HSV-1 injection, increases of 4.5-fold in TNFα and 17-fold in IL-6 were detected, whereas substantially smaller changes in TNFα and IL-6 (1.5-fold and 6.3-fold, respectively) were observed in HBSS-injected eyes. Virus-induced changes in TNFα mRNA levels occurred slightly earlier than for IL-6 because maximal levels of TNFα were detected 2 to 3 days after infection, but IL-6 peaked at day 3. Conclusions. Cultured retinal glial cells exhibit upregulated TNFα and IL-6 transcript levels after exposure to virus or inflammatory mediators. HSV-1 infection of the anterior segment of the mouse eye markedly upregulates TNFα and IL-6 mRNA levels compared to smaller responses to nonspecific inflammation. Taken together, these results identify retinal Muller cells as an intraretinal source of TNFα and IL-6 and support the potential of these resident cells to act as intraretinal modulators of immune and inflammatory responses.

Original languageEnglish
Pages (from-to)2302-2312
Number of pages11
JournalInvestigative Ophthalmology and Visual Science
Volume37
Issue number11
StatePublished - Oct 1996
Externally publishedYes

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Human Herpesvirus 1
Neuroglia
Interleukin-6
Tumor Necrosis Factor-alpha
Retina
Cytokines
Anterior Chamber
Ependymoglial Cells
Digoxigenin
Messenger RNA
Injections
Reverse Transcription
In Situ Hybridization
Anterior Eye Segment
Viruses
RNA Probes
Retinitis
Polymerase Chain Reaction
Interferon Type I
Hypoxanthine

All Science Journal Classification (ASJC) codes

  • Ophthalmology

Cite this

Herpes simplex virus type 1 alters transcript levels of tumor necrosis factor-α and interleukin-6 in retinal glial cells. / Drescher, Kristen M.; Whittum-Hudson, Judith A.

In: Investigative Ophthalmology and Visual Science, Vol. 37, No. 11, 10.1996, p. 2302-2312.

Research output: Contribution to journalArticle

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title = "Herpes simplex virus type 1 alters transcript levels of tumor necrosis factor-α and interleukin-6 in retinal glial cells",
abstract = "Purpose. Studies were performed to determine whether retinal Muller cells transcribe genes for the proinflammatory cytokines interleukin-6 (IL- 6) and tumor necrosis factor-α (TNFα). Isolated murine retinas were used to test whether these cytokines were upregulated in the retina in vivo after anterior chamber inoculation of herpes simplex virus type 1 (HSV-1). The effects of exposure to HSV-1 or interferon-γ (IFNγ) on transcript levels of these cytokines in cultured retinal glia also were examined. Methods. In situ hybridization (ISH) using digoxigenin (DIG)-labeled RNA probes was used to localize mRNA for IL-6 and TNFα in cultured retinal glial cells. Changes in IL-6 and TNFα relative transcript levels were assessed in cultured retinal glial cells using a semiquantitative approach comprised of reverse transcription-polymerase chain reaction (RT-PCR) assay at low amplification cycle number followed by slot blotting and hybridization with DIG-labeled internal sequence probes. In the murine model of herpetic retinitis, the same methods were used to compare temporal changes in relative cytokine transcript levels in retinas isolated from eyes 1 to 7 days after anterior chamber injection of live HSV-1 (KOS strain; 2 x 104 pfu/eye) or buffer with levels in retinas isolated from normal, uninjected eyes. Densitometry was used to quantify relative signal changes obtained with serial diluted samples in slot blot assays. Cytokine signal was normalized to hypoxanthine phosphoribosyl transferase signal obtained from the same cDNA samples. Results. Under baseline culture conditions, ISH and RT-PCR indicated that both IL-6 and TNFα were transcribed by cultured retinal glia. In vitro exposure to either viral (HSV-1) or inflammatory (IFNγ) stimulants increased levels of these transcripts in a time-dependent manner. Peak TNFα mRNA levels were detected 4 hours after exposure to HSV, whereas IL-6 peaked 4 hours later (increases of 10.3 and 8.7 times over baseline, respectively). Differential increases in TNFα and IL-6 transcript levels were detected in retinas isolated from BALB/c mice that received anterior chamber injections of either HSV-1 or Hanks' balanced salt solution (HBSS). By day 3 after HSV-1 injection, increases of 4.5-fold in TNFα and 17-fold in IL-6 were detected, whereas substantially smaller changes in TNFα and IL-6 (1.5-fold and 6.3-fold, respectively) were observed in HBSS-injected eyes. Virus-induced changes in TNFα mRNA levels occurred slightly earlier than for IL-6 because maximal levels of TNFα were detected 2 to 3 days after infection, but IL-6 peaked at day 3. Conclusions. Cultured retinal glial cells exhibit upregulated TNFα and IL-6 transcript levels after exposure to virus or inflammatory mediators. HSV-1 infection of the anterior segment of the mouse eye markedly upregulates TNFα and IL-6 mRNA levels compared to smaller responses to nonspecific inflammation. Taken together, these results identify retinal Muller cells as an intraretinal source of TNFα and IL-6 and support the potential of these resident cells to act as intraretinal modulators of immune and inflammatory responses.",
author = "Drescher, {Kristen M.} and Whittum-Hudson, {Judith A.}",
year = "1996",
month = "10",
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T1 - Herpes simplex virus type 1 alters transcript levels of tumor necrosis factor-α and interleukin-6 in retinal glial cells

AU - Drescher, Kristen M.

AU - Whittum-Hudson, Judith A.

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N2 - Purpose. Studies were performed to determine whether retinal Muller cells transcribe genes for the proinflammatory cytokines interleukin-6 (IL- 6) and tumor necrosis factor-α (TNFα). Isolated murine retinas were used to test whether these cytokines were upregulated in the retina in vivo after anterior chamber inoculation of herpes simplex virus type 1 (HSV-1). The effects of exposure to HSV-1 or interferon-γ (IFNγ) on transcript levels of these cytokines in cultured retinal glia also were examined. Methods. In situ hybridization (ISH) using digoxigenin (DIG)-labeled RNA probes was used to localize mRNA for IL-6 and TNFα in cultured retinal glial cells. Changes in IL-6 and TNFα relative transcript levels were assessed in cultured retinal glial cells using a semiquantitative approach comprised of reverse transcription-polymerase chain reaction (RT-PCR) assay at low amplification cycle number followed by slot blotting and hybridization with DIG-labeled internal sequence probes. In the murine model of herpetic retinitis, the same methods were used to compare temporal changes in relative cytokine transcript levels in retinas isolated from eyes 1 to 7 days after anterior chamber injection of live HSV-1 (KOS strain; 2 x 104 pfu/eye) or buffer with levels in retinas isolated from normal, uninjected eyes. Densitometry was used to quantify relative signal changes obtained with serial diluted samples in slot blot assays. Cytokine signal was normalized to hypoxanthine phosphoribosyl transferase signal obtained from the same cDNA samples. Results. Under baseline culture conditions, ISH and RT-PCR indicated that both IL-6 and TNFα were transcribed by cultured retinal glia. In vitro exposure to either viral (HSV-1) or inflammatory (IFNγ) stimulants increased levels of these transcripts in a time-dependent manner. Peak TNFα mRNA levels were detected 4 hours after exposure to HSV, whereas IL-6 peaked 4 hours later (increases of 10.3 and 8.7 times over baseline, respectively). Differential increases in TNFα and IL-6 transcript levels were detected in retinas isolated from BALB/c mice that received anterior chamber injections of either HSV-1 or Hanks' balanced salt solution (HBSS). By day 3 after HSV-1 injection, increases of 4.5-fold in TNFα and 17-fold in IL-6 were detected, whereas substantially smaller changes in TNFα and IL-6 (1.5-fold and 6.3-fold, respectively) were observed in HBSS-injected eyes. Virus-induced changes in TNFα mRNA levels occurred slightly earlier than for IL-6 because maximal levels of TNFα were detected 2 to 3 days after infection, but IL-6 peaked at day 3. Conclusions. Cultured retinal glial cells exhibit upregulated TNFα and IL-6 transcript levels after exposure to virus or inflammatory mediators. HSV-1 infection of the anterior segment of the mouse eye markedly upregulates TNFα and IL-6 mRNA levels compared to smaller responses to nonspecific inflammation. Taken together, these results identify retinal Muller cells as an intraretinal source of TNFα and IL-6 and support the potential of these resident cells to act as intraretinal modulators of immune and inflammatory responses.

AB - Purpose. Studies were performed to determine whether retinal Muller cells transcribe genes for the proinflammatory cytokines interleukin-6 (IL- 6) and tumor necrosis factor-α (TNFα). Isolated murine retinas were used to test whether these cytokines were upregulated in the retina in vivo after anterior chamber inoculation of herpes simplex virus type 1 (HSV-1). The effects of exposure to HSV-1 or interferon-γ (IFNγ) on transcript levels of these cytokines in cultured retinal glia also were examined. Methods. In situ hybridization (ISH) using digoxigenin (DIG)-labeled RNA probes was used to localize mRNA for IL-6 and TNFα in cultured retinal glial cells. Changes in IL-6 and TNFα relative transcript levels were assessed in cultured retinal glial cells using a semiquantitative approach comprised of reverse transcription-polymerase chain reaction (RT-PCR) assay at low amplification cycle number followed by slot blotting and hybridization with DIG-labeled internal sequence probes. In the murine model of herpetic retinitis, the same methods were used to compare temporal changes in relative cytokine transcript levels in retinas isolated from eyes 1 to 7 days after anterior chamber injection of live HSV-1 (KOS strain; 2 x 104 pfu/eye) or buffer with levels in retinas isolated from normal, uninjected eyes. Densitometry was used to quantify relative signal changes obtained with serial diluted samples in slot blot assays. Cytokine signal was normalized to hypoxanthine phosphoribosyl transferase signal obtained from the same cDNA samples. Results. Under baseline culture conditions, ISH and RT-PCR indicated that both IL-6 and TNFα were transcribed by cultured retinal glia. In vitro exposure to either viral (HSV-1) or inflammatory (IFNγ) stimulants increased levels of these transcripts in a time-dependent manner. Peak TNFα mRNA levels were detected 4 hours after exposure to HSV, whereas IL-6 peaked 4 hours later (increases of 10.3 and 8.7 times over baseline, respectively). Differential increases in TNFα and IL-6 transcript levels were detected in retinas isolated from BALB/c mice that received anterior chamber injections of either HSV-1 or Hanks' balanced salt solution (HBSS). By day 3 after HSV-1 injection, increases of 4.5-fold in TNFα and 17-fold in IL-6 were detected, whereas substantially smaller changes in TNFα and IL-6 (1.5-fold and 6.3-fold, respectively) were observed in HBSS-injected eyes. Virus-induced changes in TNFα mRNA levels occurred slightly earlier than for IL-6 because maximal levels of TNFα were detected 2 to 3 days after infection, but IL-6 peaked at day 3. Conclusions. Cultured retinal glial cells exhibit upregulated TNFα and IL-6 transcript levels after exposure to virus or inflammatory mediators. HSV-1 infection of the anterior segment of the mouse eye markedly upregulates TNFα and IL-6 mRNA levels compared to smaller responses to nonspecific inflammation. Taken together, these results identify retinal Muller cells as an intraretinal source of TNFα and IL-6 and support the potential of these resident cells to act as intraretinal modulators of immune and inflammatory responses.

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