Home Details
| Official Symbol of Gene | Tlr4 |
| Species | Mus musculus |
| Entrez Gene ID | 21898 |
| Official Full Name | toll-like receptor 4 |
| Also known as | Lps; Ly87; Ran/M1; Rasl2-8 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSMUSG00000039005 AllianceGenome:MGI:96824 |
| Map Location | 4 C1; 4 34.66 cM |
| Detected Sample | brain |
| Sample Detail | oligodendroglial cells |
| Detected Method | Western blot |
| Disease | MS |
| Disease subtype | N/A |
| Population | Astrocytic and microglial contamination of OPC cultures |
| Sample Size | N/A |
| Pubmed ID | 23836485 |
| Year | 2013 |
| Title | Human Endogenous Retrovirus Type W Envelope Protein Inhibits Oligodendroglial Precursor Cell Differentiation |
| Expression | up-regulation |
| Risk type | Disease risk |
| Result | We demonstrated that the ENV protein is present in close proximity to TLR4-expressing oligodendroglial precursor cells adjacent to multiple sclerosis lesions. Human and rat oligodendroglial precursor cells expressed TLR4, and the ENV-mediated activation of TLR4 led to the induction of proinflammatory cytokines and inducible nitric oxide synthase as well as the formation of nitrotyrosine groups and a subsequent reduction in myelin protein expression.Interpretation: Our findings suggest that ENV-mediated induction of nitrosative stress via activation of TLR4 results in an overall reduction of the oligodendroglial differentiation capacity, thereby contributing to remyelination failure.Therefore, pharmacological or antibody-mediated inhibition of ENV may prevent the blockade of myelin repair in the diseased or injured central nervous system. |
| Mechanism/Pathway | Human and rat oligodendroglial precursor cells expressed TLR4, and the ENV-mediated activation of TLR4 led to the induction of proinflammatory cytokines and inducible nitric oxide synthase as well as the formation of nitrotyrosine groups and a subsequent reduction in myelin protein expression |

2023,CopyRight © HMU. College of Bioinformatics Science and Technology, Harbin, China.