Araki T, Taniwaki T, Becerra S P, Chader G J, Schwartz J P
Molecular Genetics Section, Clinical Neuroscience Branch, NINDS, Bethesda, Maryland 20892-4126, USA.
J Neurosci Res. 1998 Jul 1;53(1):7-15. doi: 10.1002/(SICI)1097-4547(19980701)53:1<7::AID-JNR2>3.0.CO;2-F.
We have shown previously that pigment epithelium-derived factor (PEDF) acts as a survival factor for cerebellar granule cell neurons in culture, as well as protecting them against glutamate toxicity. In this study we have examined effects of PEDF on apoptotic cell death. We find that the granule cells die of apoptosis throughout the culture period, what we have termed "natural" apoptosis. PEDF prevents this natural apoptosis if added to immature cells, within the first 2 days in vitro (DIV), and the effect is maintained for up to DIV12. However, PEDF has no effect if added to mature cells at DIV5. Similar results are obtained when apoptosis is induced by shifting the cells from a serum- and 25 mM KCl-containing medium to serum-free medium with 5 mM KCl. PEDF most effectively blocks induced apoptosis in immature cells (DIV2) when added 24 hr prior to the change of medium, but still provides some protection when added simultaneously. However, 24 hr pretreatment with PEDF has a minimal effect when apoptosis is induced in mature DIV6 cells; addition at the same time is completely ineffective. Two polypeptide fragments of PEDF, only one of which contains the serine-protease inhibitory site, are equally active, supporting previous results which suggest that the neurotrophic effects of PEDF are not mediated by protease inhibition. We conclude that PEDF protects immature but not mature granule cells against both natural and induced apoptosis.
我们之前已经表明,色素上皮衍生因子(PEDF)在培养中可作为小脑颗粒细胞神经元的存活因子,并保护它们免受谷氨酸毒性的影响。在本研究中,我们检测了PEDF对凋亡性细胞死亡的影响。我们发现,在整个培养期间颗粒细胞死于凋亡,我们将其称为“自然”凋亡。如果在体外培养的前两天(DIV)将PEDF添加到未成熟细胞中,它可防止这种自然凋亡,并且这种作用可持续到DIV12。然而,如果在DIV5时将PEDF添加到成熟细胞中则没有效果。当通过将细胞从含有血清和25 mM KCl的培养基转移到含有5 mM KCl的无血清培养基中来诱导凋亡时,可获得类似的结果。当在培养基更换前24小时添加PEDF时,它最有效地阻断未成熟细胞(DIV2)中的诱导凋亡,但同时添加时仍可提供一些保护作用。然而,当在成熟的DIV6细胞中诱导凋亡时,用PEDF进行24小时预处理的效果最小;同时添加则完全无效。PEDF的两个多肽片段,其中只有一个含有丝氨酸蛋白酶抑制位点,具有同等活性,这支持了先前的结果,即PEDF的神经营养作用不是由蛋白酶抑制介导的。我们得出结论,PEDF可保护未成熟但不能保护成熟的颗粒细胞免受自然和诱导凋亡的影响。