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• W2135562110 endingPage "469" @default.
• W2135562110 startingPage "464" @default.
• W2135562110 abstract "Integrins are a class of cell adhesion molecules that regulate interactions between cells and their extracellular matrix (ECM). Several specific integrin receptors have been indentified in intervertebral discs, including the fibronectin-binding integrin receptors α5 β1, αv β3 and the collagen-binding integrin receptors α1 β1, α2 β1, and, αv β1. But the integrins expressions in degenerated intervertebral discs are still unknown. In our study, the expressions of α1, α2, α5, αv, β1, β3 integrin subunits, collagens, and fibronectin in normal and herniated intervertebral discs of human were determined. Specimens of human lumbar intervertebral discs were divided into 3 groups: normal discs (n = 10), protrusion (n = 15), and extrusion (n = 15). Real-time quantitative reverse transcription polymerase chain reaction (RT-PCR) and immunoprecipitation were used to evaluate the α1, α2, α5,αv, β1, and β3 integrin subunits messenger ribonucleic acid (mRNA) and protein expressions. RT-PCR was also performed to measure the mRNA level of collagen I, collagen II, and fibronectin. The expressions of α5 and β1 subunits were increased in herniated discs, especially in the discs of extrusion. But as to α1, α2, αv and β3, their expressions had no difference among the discs. Fibronectin, whose binding integrin receptor was α5 β1 was also increased. And in herniated discs, the collagen I was increased, but the collagen II was decreased. The expressions of some integrin subunits were increased in herniated discs. These results may be attributed to the interaction between cells and the ECM in the process of degeneration." @default.
• W2135562110 created "2016-06-24" @default.
• W2135562110 creator A5036934433 @default.
• W2135562110 creator A5056257531 @default.
• W2135562110 date "2008-01-01" @default.
• W2135562110 modified "2023-10-01" @default.
• W2135562110 title "Expression of Integrin Subunits in the Herniated Intervertebral Disc" @default.
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• W2135562110 doi "https://doi.org/10.1080/03008200802325425" @default.
• W2135562110 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19085247" @default.
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