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PubMed:7613621 JSONTXT

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PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T4 690-923 DRI_Outcome denotes In the present paper, we have studied the changes occurring in human primitive neuroectodermal cells following infection with human T cell lymphotropic virus type 1 (HTLV-I), a retrovirus responsible for HTLV-I-associated myelopathy.
T5 924-1024 DRI_Background denotes Infected neural cells were found to have high metalloproteinase 9 (MMP9-92 kDa gelatinase) activity.
T6 1025-1089 DRI_Background denotes MMP9 induction is dependent on HTLV-I infection of neural cells.
T7 1090-1219 DRI_Background denotes In addition, soluble factors, especially tumour necrosis factor alpha, secreted by infected cells, act as mediators of induction.
T8 1220-1319 DRI_Background denotes HTLV-I infection also induces expression of RNA coding for tissue inhibitor of metalloproteinase 2.
T9 1320-1610 DRI_Outcome denotes These observations indicate that HTLV-I infection selectively modulates the expression of molecules involved in the dynamic equilibrium between the synthesis and degradation of the neural cell matrix and leads to its remodelling, which modifies cell-cell interactions and cellular function.
T1 187-452 DRI_Background denotes Matrix-degrading proteases, including metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs), are involved in modulation of the extracellular matrix, which participates in neural cell differentiation, brain morphogenesis and tissue integrity.
T2 453-603 DRI_Background denotes Metalloproteinases and TIMPs are associated with inflammatory and degenerative processes in the central nervous system and are regulated by cytokines.
T3 604-689 DRI_Background denotes Human retroviral infections are frequently associated with neurological disturbances.