共 33 条
Hop/STI1 modulates retinal proliferation and cell death independent of PrPC
被引:18
作者:
Arruda-Carvalho, Maithe
[1
]
Njaine, Brian
[1
]
Silveira, Mariana S.
[1
]
Linden, Rafael
[1
]
Chiarini, Luciana B.
[1
]
机构:
[1] Univ Fed Rio de Janeiro, Inst Biofis, Ctr Ciencias Saude, BR-21941902 Rio De Janeiro, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
co-chaperone;
development;
retina;
proliferation;
programmed cell death;
prion protein;
D O I:
10.1016/j.bbrc.2007.07.038
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hop/STI1 is a co-chaperone adaptor protein for Hsp70/Hsp90 complexes. Hop/STI1 is found extracellularly and modulates cell death and differentiation through interaction with the prion protein (PrPc). Here, we investigated the expression of hop/STI1 and its role upon cell proliferation and cell death in the developing retina. Hop/STI1 is more expressed in developing rat retina than in the mature tissue. Hop/STI1 blocks retinal cell death in the neuroblastic layer (NBL) in a PrPC dependent manner, but failed to protect ganglion cells against axotomy-induced cell death. An antibody raised against hop/STI1 (alpha-STI1) blocked both ganglion cell and NBL cell death independent of PrPc. cAMP/PKA, ERK, PI3K and PKC signaling pathways were not involved in these effects. Hop/STI1 treatment reduced proliferation, while alpha-STI1 increased proliferation in the developing retina, both independent of PrPc. We conclude that hop/STI1 can modulate both proliferation and cell death in the developing retina independent of PrPc. (c) 2007 Elsevier Inc. All rights reserved.
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页码:474 / 480
页数:7
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