GFRα-3, a protein related to GFRα-1, is expressed in developing peripheral neurons and ensheathing cells

被引:50
作者
Widenfalk, J [1 ]
Tomac, A
Lindqvist, E
Hoffer, B
Olson, L
机构
[1] Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden
[2] NIDA, NIH, Baltimore, MD 21224 USA
[3] NICHHD, Bethesda, MD 20892 USA
关键词
ganglia; GDNF receptors; in situ hybridization; mouse; Schwann cells;
D O I
10.1046/j.1460-9568.1998.00192.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We report here the identification of a gene, termed GFR alpha-3 (glial cell line-derived neurotrophic factor family receptor alpha-3), related to GFR alpha-1 and GFR alpha-3 (also known as GDNFR-alpha and GDNFR-beta), and describe distribution of GDNF alpha-3 in the nervous system and other parts of the mouse body duping development and in the adult. GFR alpha-3 in situ hybridization signals were found mainly in the peripheral nervous system, with prominent signals in developing dorsal root and trigeminal ganglia. Sympathetic ganglia were also positive. Developing nerves manifested strong GFR alpha-3 mRNA signals, presumably generated by the Schwann cells. Olfactory ensheathing cells were also positive. Other non-neuronal cells appearing positive during development included chromaffin cells in the adrenal gland and small clusters of cells in the intestinal epithelium. In the central nervous system no robust signals could be detected at any stage investigated with the present probes. Compared with the previously described GFR alpha-1 and GFR alpha-2 mRNAs, which are widely distributed in the central nervous system and peripheral organs, the expression of GFR alpha-3 mRNA is much more restricted. The prominent expression in Schwann cells during development suggests a key role for GFR alpha-3 in the development of the peripheral nervous system. As Schwann cells are known to lack expression of the transducing RET receptor, we propose that a possible function of GFR alpha-3 during development could be to bind Schwann cell-derived GDNF-like ligands, thus presenting such molecules to growing axons.
引用
收藏
页码:1508 / 1517
页数:10
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