Extracellular matrix protein anosmin-1 modulates olfactory ensheathing cell maturation in chick olfactory bulb development

被引:5
|
作者
Hu, Youli [1 ,2 ]
Butts, Thomas [3 ,4 ,5 ]
Poopalasundaram, Subathra [3 ]
Graham, Anthony [3 ]
Bouloux, Pierre-Marc [2 ]
机构
[1] Nanjing Med Univ, Jiangsu Prov Hosp, Affiliated Hosp 1, Dept Anesthesiol, Nanjing, Jiangsu, Peoples R China
[2] UCL Med Sch, Ctr Neuroendocrinol, Royal Free Campus, London NW3 2PF, England
[3] Kings Coll London, Ctr Dev Neurobiol, London, England
[4] Univ Liverpool, Sch Life Sci, Liverpool, Merseyside, England
[5] Univ Liverpool, Dept Cellular & Mol Physiol, Liverpool, Merseyside, England
基金
中国国家自然科学基金;
关键词
astrocyte; embryo; fibroblast growth factor receptor; Kallmann syndrome; KALLMANN-SYNDROME GENE; NEURAL CREST; HEPARAN-SULFATE; SENSORY NEURONS; SCHWANN-CELL; GLIAL-CELLS; SYSTEM; EXPRESSION; SOX10; GROWTH;
D O I
10.1111/ejn.14483
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Olfactory ensheathing cells (OECs) are a specialized class of glia, wrapping around olfactory sensory axons that target the olfactory bulb (OB) and cross the peripheral nervous system/central nervous system boundary during development and continue to do so post-natally. OEC subpopulations perform distinct subtype-specific functions dependent on their maturity status. Disrupted OEC development is thought to be associated with abnormal OB morphogenesis, leading to anosmia, a defining characteristic of Kallmann syndrome. Hence, anosmin-1 encoded by Kallmann syndrome gene (KAL-1) might modulate OEC differentiation/maturation in the OB. We performed in ovo electroporation of shRNA in the olfactory placode to knock-down kal in chick embryos, resulting in abnormal OB morphogenesis and loss of olfactory sensory axonal innervation into OB. BLBP-expressing OECs appeared to form a thinner and poorly organized outmost OB layer where SOX10 expressing OECs were completely absent with emergence of GFAP-expressing OECs. Furthermore, in embryonic day 10 chick OB explant cultures, GFAP expression in OECs accumulating along the OB nerve layers was dramatically reduced by recombinant anosmin-1. We then purified immature OECs from embryonic day 10 chick OB. These cells express GFAP after 7 days in vitro, exhibiting a multipolar morphology. Overexpression of chick anosmin, exogenous anosmin-1 or FGF2 could inhibit GFAP expression with cells presenting elongated morphology, which was blocked by the FGF receptor inhibitor Su5402. These data demonstrate that anosmin-1 functions via FGF signalling in regulating OEC maturation, thereby providing a permissive glial environment for axonal innervation into the OB during development.
引用
收藏
页码:3472 / 3486
页数:15
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