TY - JOUR
T1 - Conversion of mammalian Müller glial cells into a neuronal lineage by in vitro aggregate-culture
AU - Kubota, Akira
AU - Nishida, Kohji
AU - Nakashima, Kinichi
AU - Tano, Yasuo
N1 - Funding Information:
We are grateful to Professor Masaru Okabe (Research Institute for Microbial Diseases, Osaka University) for kindly gifting green fluorescent protein (GFP)-transgenic rats. This study was supported by Grant-in-Aid 18390468 for scientific research from the Ministry of Education, Science, Culture, and Sports of Japan.
PY - 2006/12/15
Y1 - 2006/12/15
N2 - Mammalian Müller glial cells are major glial cells in the retina. Here we report that these glial cells can be redirected towards a neuronal lineage by an aggregate-culture in vitro. Rat and macaque Müller glial cells did not express neuronal markers except after transfer to adhesive conditions. Furthermore, this expression could only take place in the presence of platelet-derived growth factor and valproic acid. We compared a normal monolayer-culture and an aggregate-culture, and rat Müller glial cells could only differentiate into neurons under non-adhesive conditions. However, Müller glial cells did not express the photoreceptor markers in vitro. After transplantation into the subretinal space, a retina-specific niche, rat Müller glial cells expressed the photoreceptor-specific marker, opsin (RET-P1). We demonstrate the potential of mammalian Müller glial cells as a source of photoreceptors, which may possibly contribute to the treatment of degenerative retinal diseases such as retinitis pigmentosa.
AB - Mammalian Müller glial cells are major glial cells in the retina. Here we report that these glial cells can be redirected towards a neuronal lineage by an aggregate-culture in vitro. Rat and macaque Müller glial cells did not express neuronal markers except after transfer to adhesive conditions. Furthermore, this expression could only take place in the presence of platelet-derived growth factor and valproic acid. We compared a normal monolayer-culture and an aggregate-culture, and rat Müller glial cells could only differentiate into neurons under non-adhesive conditions. However, Müller glial cells did not express the photoreceptor markers in vitro. After transplantation into the subretinal space, a retina-specific niche, rat Müller glial cells expressed the photoreceptor-specific marker, opsin (RET-P1). We demonstrate the potential of mammalian Müller glial cells as a source of photoreceptors, which may possibly contribute to the treatment of degenerative retinal diseases such as retinitis pigmentosa.
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U2 - 10.1016/j.bbrc.2006.10.072
DO - 10.1016/j.bbrc.2006.10.072
M3 - Article
C2 - 17070773
AN - SCOPUS:33750494538
SN - 0006-291X
VL - 351
SP - 514
EP - 520
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -