Basement membrane-like matrix sponge for the three-dimensional proliferation culture of differentiated retinal horizontal interneurons

被引:6
作者
Ajioka, Itsuki [1 ,2 ]
Ichinose, Shizuko [3 ]
Nakajima, Kazunori [4 ]
Mizusawa, Hidehiro [1 ,5 ]
机构
[1] Tokyo Med & Dent Univ, Ctr Brain Integrat Res, Tokyo 1138510, Japan
[2] Keio Univ, Sch Med, Ctr Integrated Med Res, Shinjuku Ku, Tokyo 1608582, Japan
[3] Tokyo Med & Dent Univ, Res Ctr Med & Dent Sci, Tokyo 1138510, Japan
[4] Keio Univ, Sch Med, Dept Anat, Shinjuku Ku, Tokyo 1608582, Japan
[5] Tokyo Med & Dent Univ, Dept Neurol & Neurol Sci, Tokyo 1138510, Japan
基金
日本科学技术振兴机构;
关键词
Neural cell; ECM (extra-cellular matrix); Cell proliferation; Cell culture; TISSUE-CULTURE; CELL-CYCLE; NEURONAL MIGRATION; RETINOBLASTOMA; MECHANISMS; SCAFFOLDS; NEOCORTEX; ORIGIN; MODEL; GENE;
D O I
10.1016/j.biomaterials.2011.04.062
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
As the neurons in the central nervous system (CNS) form a neuronal network in a three-dimensional (3D) manner, a 3D proliferation culture system for differentiated neurons has been desired. Although differentiated neurons were previously thought to never proliferate, differentiated horizontal interneurons of Rb-/-; p107+/-; p130-/- (p107-single) retina clonally proliferated without dedifferentiation in vivo Ill. In the present study, we developed a basement membrane-like matrix sponge (BM-sponge) for the 3D proliferation culture of differentiated horizontal interneurons. p107-single horizontal interneurons, but not other types of retinal neurons, proliferated in the BM-sponge in a 3D manner. These interneurons expressed presynaptic marker and developed synaptic vesicles. These data demonstrated that p107-single horizontal interneurons cultured in the BM-sponge proliferate while maintaining their differentiated features. We described here the 3D proliferation culture system for differentiated neurons. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5765 / 5772
页数:8
相关论文
共 33 条
[11]  
GASSER UE, 1990, J NEUROSCI, V10, P1276
[12]   ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428
[13]   CELL-DEATH AND THE CELL-CYCLE - A RELATIONSHIP BETWEEN TRANSFORMATION AND NEURODEGENERATION [J].
HEINTZ, N .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (05) :157-159
[14]   Cell cycle regulation in the postmitotic neuron: oxymoron or new biology? [J].
Herrup, Karl ;
Yang, Yan .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (05) :368-378
[15]   MORPHOLOGICAL AND PHYSIOLOGICAL PROPERTIES OF NEURONS AND GLIAL CELLS IN TISSUE CULTURE [J].
HILD, W ;
TASAKI, I .
JOURNAL OF NEUROPHYSIOLOGY, 1962, 25 (02) :277-&
[16]   TO DO TISSUE-CULTURE IN 2 OR 3 DIMENSIONS - THAT IS THE QUESTION [J].
HOFFMAN, RM .
STEM CELLS, 1993, 11 (02) :105-111
[17]   Fabrication of porous gelatin scaffolds for tissue engineering [J].
Kang, HW ;
Tabata, Y ;
Ikada, Y .
BIOMATERIALS, 1999, 20 (14) :1339-1344
[18]   The use of 3-D cultures for high-throughput screening: The multicellular spheroid model [J].
Kunz-Schughart, LA ;
Freyer, JP ;
Hofstaedter, F ;
Ebner, R .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (04) :273-285
[19]   COLLAGEN-COATED CELLULOSE SPONGE - 3-DIMENSIONAL MATRIX FOR TISSUE CULTURE OF WALKER TUMOR 256 [J].
LEIGHTON, J ;
JUSTH, G ;
ESPER, M .
SCIENCE, 1967, 155 (3767) :1259-&
[20]   Origin of GABAergic neurons in the human neocortex [J].
Letinic, K ;
Zoncu, R ;
Rakic, P .
NATURE, 2002, 417 (6889) :645-649