Evidence map›Paper›PMID 16896914›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2007

T-bet expression in the iris and spleen parallels disease expression during endotoxin-induced uveitis.

Bing Li, Peizeng Yang, Liqun Chu, Hongyan Zhou, Xiangkun Huang, Lianxiang Zhu, Aize Kijlstra

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Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
–field-weighted citation impact, top 79% of its field
1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Dynamic DNA Methylation Changes ofMediators of inflammation · 2018
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4 · The record

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5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Bing LiZhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, 510060, People's Republic of China.
Peizeng Yang
Liqun Chu
Hongyan Zhou
Xiangkun Huang
Lianxiang Zhu
Aize Kijlstra
Sun Yat-sen University · CNMaastricht University · NLMinistry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT lymphocytes have been implicated in the development of endotoxin-induced uveitis (EIU). T-bet is a Th1 cell-specific transcription factor that is involved in differentiation and effector functions. The aim of this study was to investigate kinetics of T-bet expression at the mRNA and protein levels during EIU using real-time PCR and whole-mount immunohistochemistry.

methodsA single footpad injection of 200 mug of lipopolysaccharide (LPS) was administered to male Wistar rats in order to induce EIU. Clinical changes were followed by slit-lamp examination. The expression of T-bet mRNA in the spleen was evaluated 0, 8, 16, 24, 48, and 96 h after LPS injection using real-time PCR. Immunohistochemistry was performed on the iris whole-mounts as well as on frozen sections of the spleen to evaluate T-bet protein expression. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) was performed on the iris whole-mounts to assay apoptotic cells.

resultsUveitis was observed in all rats that received LPS. T-bet(+) cells and TUNEL(+) cells in the iris whole-mounts showed a similar pattern in cell number and distribution and both types of cells were observed at 8 h, significantly increased 24 h, and decreased 48 h after LPS injection. T-bet expression at both the mRNA and protein levels in spleen also paralleled ocular inflammation. It was weakly detectable after 0 h, increased after 8 h (index 1.3, T-bet(+) cells OD 17.43+/-2.15), reached its peak after 24 h (index 4.00, OD 53.52+/-4.00), and decreased 48 h following LPS injection (index 1.38, OD 25.75+/-2.45).

conclusionsThe results show that T-bet expression in both the iris and the spleen, and in apoptotic cells in the iris parallel the severity of intraocular inflammation after systemic LPS administration. These results suggest that T-bet may play a significant role in the dynamics of EIU.

Indexed as

AnimalsApoptosisGene Expression RegulationImmunohistochemistryIn Situ Nick-End LabelingIrisLipopolysaccharidesMaleRatsRats, WistarReverse Transcriptase Polymerase Chain ReactionRNA, MessengerSalmonella typhimuriumSpleenT-bet Transcription FactorT-Box Domain ProteinsLipopolysaccharidesRNA, MessengerT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID16896914
OpenAlexW2145138299

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.