Effects of Muller Glia on Cell Survival and Neuritogenesis in Adult Porcine Retina In Vitro

• Published in: Investigative ophthalmology & visual science Vol. 43; no. 12; pp. 3735 - 3743
• Main Authors: Garcia, Monica, Forster, Valerie, Hicks, David, Vecino, Elena
• Format: Journal Article
• Language: English
• Published: Rockville, MD ARVO 01.12.2002; Association for Research in Vision and Ophtalmology
• Subjects: Animals; Biological and medical sciences; Brain-Derived Neurotrophic Factor - pharmacology; Cell Size; Cell Survival - drug effects; Cells, Cultured; Coculture Techniques; Eye and associated structures. Visual pathways and centers. Vision; Fluorescent Antibody Technique, Indirect; Fundamental and applied biological sciences. Psychology; Glial Cell Line-Derived Neurotrophic Factor; Nerve Growth Factors - pharmacology; Neurites - physiology; Neuroglia - physiology; Retinal Ganglion Cells - cytology; Retinal Ganglion Cells - drug effects; Swine; Vertebrates: nervous system and sense organs; Cell culture; Glial cell; Retina; Muller cell; Neuroprotective agent; In vitro; Survival; Visual system; Vertebrata; Mammalia; Swine; Animal; Adult animal; Physiology; Artiodactyla; Brain derived neurotrophic factor; Ungulata
• ISSN: 0146-0404; 1552-5783

To examine the effects of glia-derived and brain-derived neurotrophic factors on survival and morphology of cultured retinal ganglion cells (RGCs) from adult porcine retina. Adult porcine retinas were dissociated and cultured in different conditions: (1) on laminin- and poly-D-lysine-coated coverslips in chemically defined medium (CDM); (2) on laminin- and poly-D-lysine-coated coverslips in CDM supplemented with brain-derived neurotrophic factor (BDNF); (3) in confluent monolayer cultures of retinal Müller glia (RMG) in CDM; (4) in 1-day cultures of RMG in CDM; (5) in fixed RMG cultures in CDM; and (6) in laminin-poly-D-lysine substrate in conditioned medium obtained from RMG. RGCs were classified on the basis of the size, number of neurites, and length of the neurites, and the survival of the RGCs was assayed after each treatment. Confluent RMG substrates and RMG-conditioned medium significantly increased the survival of cultured porcine RGCs. Moreover, these two conditions increased the size of the RGCs and enhanced growth and elongation of the neurite. Addition of BDNF to the culture medium or use of 1-day cultured RMG as a substrate did not modify survival but increased the size, neurite number, and neurite length in the RCGs. These findings demonstrate that factor(s) secreted by RMG exert beneficial effects on survival of adult RGCs and neurite regeneration in vitro and may constitute effective agent(s) for neuroprotection of RGC.