Glial-cell-line-derived neurotrophic factor induces nerve fibre formation in primary cultures of adrenal chromaffin cells

被引:0
作者
Förander P. [1 ]
Broberger C. [1 ]
Strömberg I. [1 ]
机构
[1] Department of Neuroscience, Karolinska Institutet, S-171 77 Stockholm, Berzelius Väg 7
关键词
Chromaffin cells; GDNF; GFRα; Rat (Sprague Dawley); TGFβ;
D O I
10.1007/s004410100401
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学科分类号
摘要
Neurotrophic factors, such as nerve growth factor (NGF), have been shown to promote the differentiation of neural crest neuroblasts into sympathetic neurons, whereas glucocorticoids promote the endocrine phenotype of adrenal medullary chromaffin cells. This pluripotency is preserved to some extent in adult chromaffin cells, with NGF and other neurotrophic factors influencing the differentiation of these cells. In this study, the effects of glial cell line-derived neurotrophic factor (GDNF) on explanted chromaffin tissue have been investigated. The localization of mRNAs corresponding to the two components of the GDNF receptor, GDNF family receptor alpha 1 (GFRα1) and Ret, were demonstrated in adult adrenal medullary ganglion cells. GFRα1 mRNA was expressed in explanted chromaffin tissue at levels dependent on the presence of serum in the medium but decreased on the addition of blocking antibodies against transforming growth factor beta (TGFβ). However, TGFβ1 (1 ng/ml) did not upregulate GFRα1 mRNA expression when added to serum-free medium. GDNF induced neurite formation from chromaffin cells, as measured by the ratio of neurite-bearing versus total number of chromaffin cells in primary cultures of adult adrenal medulla. The most potent dose inducing neurites from chromaffin cells was 100 ng/ml GDNF. However, this dose was not as efficient as that seen when chromaffin cells were stimulated with NGF (100 ng/ml). Thus, adrenal medullary cells express mRNAs for the GDNF receptor components Ret and GFRα1, increase their expression upon being cultured in serum-containing medium and respond to GDNF treatment with an increase in the number of cells that develop nerve processes.
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页码:43 / 51
页数:8
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共 56 条
[1]  
Anderson D.J., Carnahan J., Michelsohn A., Patterson P.H., Antibody markers identify a common progenitor to sympathetic neurons and chromaffin cells in vivo and reveal the timing of commitment to neuronal differentiation in the sympathoad-renal lineage, J Neurosci, 11, pp. 3507-3519, (1991)
[2]  
Arenas E., Trupp M., Akerud P., Ibanez C.F., GDNF prevents degeneration and promotes the phenotype of brain noradrenergic neurons in vivo, Neuron, 15, pp. 1465-1473, (1995)
[3]  
Beck K.D., Valverde J., Alexi T., Poulsen K., Moffat B., Vandlen R.A., Rosenthal A., Hefti F., Mesencephalic dopaminergic neurons protected by GDNF from axotomy-induced degeneration in the adult brain, Nature, 373, pp. 339-341, (1995)
[4]  
Benett D.L.H., Michael G.J., Ramachandran N., Munson J.B., Averill S., Yan Q., McMahon S.B., Priestley J.V., A distinct subgroup of small DRG cells express GDNF receptor components and GDNF is protective for these neurons after nerve injury, J Neurosci, 18, pp. 3059-3072, (1998)
[5]  
Bohn M.C., Goldstein M., Black I., Role of glucocorticoids in expression of the adrenergic phenotype in rat embryonic adrenal gland, Dev Biol, 82, pp. 1-10, (1981)
[6]  
Buj-Bello A., Buchman V., Horton A., Rosenthal A., Davies A., GDNF is an age-specific survival factor for sensory and autonomic neurons, Neuron, 15, pp. 821-828, (1995)
[7]  
Cacalano G., Farinas I., Wang L.-C., Hagler K., Forgie A., Moore M., Armanini M., Phillips H., Ryan A.M., Reichardt L.F., Hynes M., Davies A., Rosenthal A., GFRa1 is an essential receptor component for GDNF in the developing nervous system and kidney, Neuron, 21, pp. 53-62, (1998)
[8]  
Chalazonitis A., Rothman T.P., Chen J., Gershon M.D., Age dependent differences in the effects of GDNF and NT-3 on the development of neurons and glia from neural crest-derived precursors immunoselected from the fetal rat gut: Expression of GFRa1 in vitro and in vivo, Dev Biol, 204, pp. 385-406, (1998)
[9]  
Chiariello M., Visconti R., Carlomagno F., Melillo R.M., Bucci C., De Franciscis V., Fox G.M., Jing S., Coso O.A., Gutkind J.S., Fusco A., Santoro M., Signaling of ret receptor tyrosine kinase through the c-jun NH2-terminal protein kinase (JNKs): Evidence for a divergence of the ERKs and JNKs pathways induced by ret, Oncogene, 16, pp. 2435-2445, (1998)
[10]  
Coupland R.E., The natural history of the adrenal gland, (1965)