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Pigment epithelium-derived factor promotes the survival and differentiation of developing spinal motor neurons

✍ Scribed by Houenou, Lucien J.; D'Costa, Anselm P.; Li, Linxi; Turgeon, Victoria L.; Enyadike, Cyril; Alberdi, Elena; Becerra, S. Patricia


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
243 KB
Volume
412
Category
Article
ISSN
0021-9967

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✦ Synopsis


Pigment epithelium-derived factor (PEDF) is a member of the serine protease inhibitor (serpin) superfamily that has been shown previously to promote the survival and/or differentiation of rat cerebellar granule neurons and human retinoblastoma cells in vitro. However, in contrast to most serpins, PEDF has no inhibitory activity against any known proteases, and its described biological activities do not appear to require the serpin-reactive loop located toward the carboxy end of the polypeptide. Because another serpin, protease nexin-1, has been shown to promote the in vivo survival and growth of motor neurons, the authors investigated the potential neurotrophic effects of PEDF on spinal cord motor neurons in highly enriched cultures and in vivo after injury. Here, it is shown that native bovine and recombinant human PEDF promoted the survival and differentiation (neurite outgrowth) of embryonic chick spinal cord motor neurons in vitro in a dose-dependent manner. A truncated form of PEDF that lacks Ϸ62% of the carboxy end of the polypeptide comprising the homologous serpin-reactive loop also exhibited neurotrophic activities similar to those of the full-length protein. Furthermore, the data here showed that PEDF was transported retrogradely and prevented the death and atrophy of spinal motor neurons in the developing neonatal mouse after axotomy. These results indicate that PEDF exerts trophic effects on motor neurons, and, together with previous reports, these findings suggest that this protein may be useful as a pharmacologic agent to promote the development and maintenance of motor neurons.


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## Abstract Microarray analyses demonstrated that a variety of genes was affected by treatment of cerebellar granule cell neurons with the neurotrophic factor pigment epithelium‐derived factor (PEDF). The genes for neurotrophins, glial cell‐derived neurotrophic factor (GDNF), and their receptors we