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miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1
by
Li, Shanxiang
, He, Hong
, Chen, Yanting
in
631/250
/ 631/553
/ Aged
/ Animal research
/ Animals
/ Chromosome 3
/ Cytokines
/ Cytokines - genetics
/ Cytokines - metabolism
/ Demography
/ Diabetes
/ Disease Models, Animal
/ Endophthalmitis
/ Endophthalmitis - genetics
/ Endophthalmitis - metabolism
/ Endophthalmitis - pathology
/ Enzyme-linked immunosorbent assay
/ Experiments
/ Female
/ Humanities and Social Sciences
/ Humans
/ Infectious endophthalmitis
/ Inflammation
/ Inflammation - genetics
/ Inflammation - metabolism
/ Inflammatory response
/ Lipopolysaccharides
/ Male
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ miR-27a-3p
/ miRNA
/ multidisciplinary
/ Ophthalmology
/ Pathogens
/ Rats
/ Rats, Sprague-Dawley
/ Retina
/ Reverse transcription
/ Science
/ Science (multidisciplinary)
/ TSC1
/ TSC1 gene
/ Tuberous sclerosis
/ Tuberous Sclerosis Complex 1 Protein - genetics
/ Tuberous Sclerosis Complex 1 Protein - metabolism
/ Tumor necrosis factor-TNF
2024
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miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1
by
Li, Shanxiang
, He, Hong
, Chen, Yanting
in
631/250
/ 631/553
/ Aged
/ Animal research
/ Animals
/ Chromosome 3
/ Cytokines
/ Cytokines - genetics
/ Cytokines - metabolism
/ Demography
/ Diabetes
/ Disease Models, Animal
/ Endophthalmitis
/ Endophthalmitis - genetics
/ Endophthalmitis - metabolism
/ Endophthalmitis - pathology
/ Enzyme-linked immunosorbent assay
/ Experiments
/ Female
/ Humanities and Social Sciences
/ Humans
/ Infectious endophthalmitis
/ Inflammation
/ Inflammation - genetics
/ Inflammation - metabolism
/ Inflammatory response
/ Lipopolysaccharides
/ Male
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ miR-27a-3p
/ miRNA
/ multidisciplinary
/ Ophthalmology
/ Pathogens
/ Rats
/ Rats, Sprague-Dawley
/ Retina
/ Reverse transcription
/ Science
/ Science (multidisciplinary)
/ TSC1
/ TSC1 gene
/ Tuberous sclerosis
/ Tuberous Sclerosis Complex 1 Protein - genetics
/ Tuberous Sclerosis Complex 1 Protein - metabolism
/ Tumor necrosis factor-TNF
2024
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miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1
by
Li, Shanxiang
, He, Hong
, Chen, Yanting
in
631/250
/ 631/553
/ Aged
/ Animal research
/ Animals
/ Chromosome 3
/ Cytokines
/ Cytokines - genetics
/ Cytokines - metabolism
/ Demography
/ Diabetes
/ Disease Models, Animal
/ Endophthalmitis
/ Endophthalmitis - genetics
/ Endophthalmitis - metabolism
/ Endophthalmitis - pathology
/ Enzyme-linked immunosorbent assay
/ Experiments
/ Female
/ Humanities and Social Sciences
/ Humans
/ Infectious endophthalmitis
/ Inflammation
/ Inflammation - genetics
/ Inflammation - metabolism
/ Inflammatory response
/ Lipopolysaccharides
/ Male
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Middle Aged
/ miR-27a-3p
/ miRNA
/ multidisciplinary
/ Ophthalmology
/ Pathogens
/ Rats
/ Rats, Sprague-Dawley
/ Retina
/ Reverse transcription
/ Science
/ Science (multidisciplinary)
/ TSC1
/ TSC1 gene
/ Tuberous sclerosis
/ Tuberous Sclerosis Complex 1 Protein - genetics
/ Tuberous Sclerosis Complex 1 Protein - metabolism
/ Tumor necrosis factor-TNF
2024
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miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1
Journal Article
miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1
2024
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Overview
Infectious endophthalmitis (IE) poses a significant threat to vision. This study aimed to explore the impact of microRNA (miR)-27a-3p on inflammation in IE. A rat model was developed through intravitreal injection of lipopolysaccharide. Clinical and demographic data were collected for 54 participants: 31 diagnosed with IE and 23 non-infectious patients with idiopathic macular holes. Expression levels of miR-27a-3p and inflammatory genes were quantified via reverse transcription quantitative polymerase chain reaction. Concentrations of inflammatory cytokines in human vitreous samples were measured using enzyme-linked immunosorbent assay. In vitro studies were conducted to explore the target gene of miR-27a-3p. The final animal experiments further verified the role of miR-27a-3p and tuberous sclerosis complex (TSC)1 in inflammatory responses. Results showed that miR-27a-3p was elevated in LPS-treated rats and IE patients. Thirty-one IE patients were divided into the High (n = 15) and Low (n = 16) groups according to the expression of miR-27a-3p. No significant differences were observed in baseline clinical and demographic characteristics between the control and IE patient groups. Pro-inflammatory cytokine mRNA levels and concentrations were notably increased in both LPS-treated rats and the High group of patients. Besides, results showed that TSC1 is a target gene of miR-27a-3p. Moreover, TSC1 inhibition promoted inflammation in rat vitreous samples. In summary, our findings suggested that miR-27a-3p exacerbated inflammatory responses in IE though targeting TSC1, offering novel insights for potential therapeutic strategies targeting miR-27a-3p in the clinical management of IE.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 631/553
/ Aged
/ Animals
/ Diabetes
/ Endophthalmitis - metabolism
/ Enzyme-linked immunosorbent assay
/ Female
/ Humanities and Social Sciences
/ Humans
/ Male
/ miRNA
/ Rats
/ Retina
/ Science
/ TSC1
/ Tuberous Sclerosis Complex 1 Protein - genetics
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