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Publication : Megalin deficiency induces critical changes in mouse spinal cord development.

First Author  Wicher G Year  2008
Journal  Neuroreport Volume  19
Issue  5 Pages  559-63
PubMed ID  18388738 Mgi Jnum  J:136621
Mgi Id  MGI:3796706 Doi  10.1097/WNR.0b013e3282f94267
Citation  Wicher G, et al. (2008) Megalin deficiency induces critical changes in mouse spinal cord development. Neuroreport 19(5):559-63
abstractText  Low density lipoprotein receptor-related protein, megalin, is a multifunctional lipoproptein receptor expressed by absorptive epithelia for endocytosis of numerous ligands. Megalin is widely expressed during embryonic life and is essential for development of the nervous system as evidenced by severe forebrain abnormalities in megalin (-/-). Here, we investigated the influence of megalin deficiency on prenatal spinal cord development in mice. In contrast to wild-type mice, cells expressing Olig2 and NG2, that is, oligodendroglial precursor cells, are absent from embryonic stage E16 in megalin (-/-) mice. At the end of prenatal development, there is a failure in vertebral development, and the number of astrocytes are markedly reduced in megalin (-/-) mice. These findings indicate that megalin is essential in astro-oligodendroglial interactions during development of the spinal cord.
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