Id |
Subject |
Object |
Predicate |
Lexical cue |
T1 |
112-204 |
DRI_Challenge |
denotes |
Gliotoxic responses complicate human eye diseases, the causes of which often remain obscure. |
T2 |
205-249 |
DRI_Approach |
denotes |
Here, we activated Müller cells (MCs) by the |
T3 |
278-420 |
DRI_Approach |
denotes |
(AAA) and assayed possible protective effects by pigment epithelium-derived factor (PEDF) in RPE-free retinal explants of the E6 chick embryo. |
T4 |
421-570 |
DRI_Background |
denotes |
These models are suited to analyze gliotoxic reactions in vitro, since the avian retina contains only Müller cells (MCs) as glial components, and the |
T5 |
589-623 |
DRI_Background |
denotes |
are devoid of a major PEDF source. |
T6 |
624-783 |
DRI_Background |
denotes |
ChAT- and AChE-immunohistochemistry (IHC) revealed that AAA treatment disrupted the differentiation of cholinergic amacrine cells in the inner plexiform layer. |
T7 |
784-915 |
DRI_Background |
denotes |
At the applied concentration of 1 mM AAA, apoptosis of MCs was slightly increased, as shown by TUNEL and caspase-3 activity assays. |
T8 |
916-1070 |
DRI_Background |
denotes |
Concomitantly, cell-free gaps emerged in the middle of the retina, where MCs were swollen and amassed glutamine synthetase (shown by GS and Vimentin IHC). |
T9 |
1071-1186 |
DRI_Background |
denotes |
AAA treatment strongly activated MCs, as shown by GFAP IHC, and by an increase of stress-related catalase activity. |
T10 |
1187-1277 |
DRI_Outcome |
denotes |
Remarkably, nearly all effects of AAA on MCs were effectively counter-balanced by 50 ng/ml |
T11 |
1295-1321 |
DRI_Outcome |
denotes |
, as also shown by RT-PCR. |
T12 |
1322-1425 |
DRI_Approach |
denotes |
These findings suggest that supplementation with PEDF can protect the retina against gliotoxic attacks. |
T13 |
1426-1516 |
DRI_Approach |
denotes |
Further studies should establish whether PEDF similarly protects a gliotoxic human retina. |