Extracellular matrix proteins increase the expression of pro-TRH and pro-protein convertase PC1 in fetal hypothalamic neurons in vitro

Developmental Brain Research

Volumn 120, Issue 1, 2000, Pages 49-56

  Niquet, Jerome ^a   Pérez Martínez, Leonor ^a   Guerra, Magdalena ^a   Grouselle, Dominique ^b   Joseph Bravo, Patricia ^a   Charli, Jean Louis ^a  

^a INSTITUTO DE BIOTECNOLOGÍA   (Mexico)

^b GDR 116 Ctr Natl Rech S   (France)

Author keywords

Fibronectin; Hypothalamus; Laminin; Pro protein convertase PC1; Pro TRH; Tenascin C; TRH; Vitronectin

Indexed keywords

FIBRONECTIN; LAMININ; MESSENGER RNA; POLYLYSINE; PRO PROTEIN CONVERTASE PC1; PRO PROTIRELIN; PROTEIN PRECURSOR; PROTIRELIN; SCLEROPROTEIN; TENASCIN; UNCLASSIFIED DRUG; VITRONECTIN;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; EXTRACELLULAR MATRIX; FETUS; GLIA CELL; HYPOTHALAMUS; NERVE FIBER GROWTH; NONHUMAN; PEPTIDE SYNTHESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; RNA TRANSLATION;

ANIMALS; ASPARTIC ENDOPEPTIDASES; CELL SURVIVAL; CELLS, CULTURED; EXTRACELLULAR MATRIX PROTEINS; FETUS; FIBRONECTINS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HYPOTHALAMUS; LAMININ; NEURONS; PROPROTEIN CONVERTASES; PROTEIN BIOSYNTHESIS; PROTEIN PRECURSORS; PYRROLIDONECARBOXYLIC ACID; RADIOIMMUNOASSAY; RATS; RATS, WISTAR; RNA, MESSENGER; TENASCIN; THYROTROPIN-RELEASING HORMONE; VITRONECTIN;

ANIMALIA;

EID: 0342514545     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-3806(99)00190-X     Document Type: Article

References (33)

1. Adler R., Jerdan J., Hewitt A.T. Responses of cultured neural retinal cells to substratum-bound laminin and other extracellular matrix molecules. Dev. Biol. 112:1985;100-114.
2. Benecke B.J., Ben-Ze'ev A., Penman S. The control of mRNA production, translation and turnover in suspended and reattached anchorage-dependent fibroblasts. Cell. 14:1978;931-939.
3. Bixby J.L., Harris W.A. Molecular mechanisms of axons growth and guidance. Ann. Rev. Cell Biol. 7:1991;117-159.
4. Bruhn T.O., Huang S.S., Vaslet C., Nillni E.A. Glucocorticoids modulate the biosynthesis and processing of prothyrotropin releasing hormone (proTRH). Endocrine. 9:1998;143-152.
5. Burgunder J.M., Taylor T. Ontogeny of thyrotropin-releasing hormone gene expression in the rat diencephalon. Neuroendocrinology. 49:1989;631-640.
6. Charli J.L., Cruz C., Redondo J.L., Guerra C., Joseph-Bravo P. Homologous conditioned medium enhances expression of TRH in hypothalamic neurons in primary culture. Dev. Brain Res. 89:1995;155-160.
7. Covarrubias L., Uribe R.M., Méndez M., Charli J.L., Joseph-Bravo P. Neuronal TRH synthesis: developmental and circadian TRH mRNA levels. Biochem. Biophys. Res. Commun. 151:1988;615-622.
8. Faissner A., Kruse J. J1/tenascin-C is a repulsive substrate for central nervous system neurons. Neuron. 5:1990;627-637.
9. Faivre-Bauman A., Loudes C., Barret A., Patte C., Tixier-Vidal A. Ontogenesis of peptidylglycyl alpha-amidation activity in the mouse hypothalamus in vivo and in serum-free medium cultures. Relation with thyroliberin (TRH) accumulation and release in vitro. Brain Res. 468:1988;261-267.
10. Faivre-Bauman A., Puymirat J., Loudes C., Barret A., Tixier-Vidal A. Laminin promotes attachment and neurite elongation of fetal hypothalamic neurons grown in serum-free medium. Neurosci. Lett. 44:1984;83-89.
11. Farmer S.R., Ben-Ze'ev A., Penman S. Altered translability of messenger RNA from suspended anchorage-dependent fibroblasts: reversal upon cell attachment to a surface. Cell. 15:1978;627-637.
12. Friedman T.C., Loh Y.P., Cawley N.X., Birch N.P., Huang S.S., Jackson I.M.D., Nillni E.A. Processing of prothyrotropin-releasing hormone (Pro-TRH) by bovine intermediate lobe secretory vesicle membrane PC1 and PC2 enzymes. Endocrinology. 136:1995;4462-4472.
13. Fukamauchi F., Aihara O., Kusakabe M. Reduced mRNA expression of neuropeptide Y in the limbic system of tenascin gene disrupted mouse brain. Neuropeptides. 32:1998;265-268.
14. Fukamauchi F., Mataga N., Wang Y.J., Sato S., Yoshiki A., Kusakabe M. Tyrosine hydroxylase activity and its mRNA level in dopaminergic neurons of tenascin gene knockout mouse. Biochem. Biophys. Res. Commun. 231:1997;356-359.
15. Grouselle D., Destombes J., Barret A., Pradelles P., Loudes C., Tixier-Vidal A., Faivre-Bauman A. Evidence for high molecular weight immunoreactive thyrotropin releasing hormone (TRH) precursor forms in the developing mouse hypothalamus. Simultaneous immunolocalization with TRH in cultured neurons. Endocrinology. 126:1990;2454-2464.
16. + neurons, Soc. Neurosci. (USA) abstract, 1999.
17. Howe A., Aplin A.E., Alahari S.K., Juliano R.L. Integrin signaling and cell growth control. Curr. Opin. Cell Biol. 10:1998;220-231.
18. R.M. Lechan, R. Toni, Thyrotropin-releasing hormone (TRH) neuronal systems in the central nervous system, in: C.B. Nemeroff (Ed.), Neuroendocrinology, CRC Press, Boca Raton, FL, 1992, pp. 279-330.
19. Letourneau P.C., Condic M.L., Snow D.M. Interactions of developing neurons with the extracellular matrix. J. Neurosci. 14:1994;915-928.
20. Lochter A., Vaughan L., Kaplony A., Prochiantz A., Schachner M., Faissner A. J1/tenascin-C in substrate-bound and soluble form displays contrary effects on neurite outgrowth. J. Cell Biol. 113:1991;1159-1171.
21. Manthorpe M., Engvall E., Ruoslahti E., Longo F.M., Davis G.E., Varon S. Laminin promotes neuritic regeneration from cultured peripheral and central neurons. J. Cell Biol. 97:1983;1882-1890.
22. Nemeskeri A., Grouselle D., Faivre-Bauman A., Tixier-Vidal A. Developmental changes of thyroliberin (TRH) in the rat brain. Neurosci. Lett. 53:1985;279-284.
23. Neugebauer K.M., Emmet C.J., Venstrom K.A., Reichardt L.F. Vitronectin and thrombospondin promote retinal neurite outgrowth: developmental regulation and role of integrins. Neuron. 6:1991;345-358.
24. Nillni E.A., Friedman T.C., Todd R.B., Birch N.P., Loh Y.P., Jackson I.M.D. Pro-thyrotropin-releasing hormone processing by recombinant PC1. J. Neurochem. 65:1995;2462-2472.
25. Nillni E.A., Luo L.G., Jackson I.M.D., McMillan P. Identification of the thyrotropin-releasing hormone precursor, its processing products, and its coexpression with convertase 1 in primary cultures of hypothalamic neurons: anatomic distribution of PC1 and PC2. Endocrinology. 137:1996;5651-5661.
26. Pérez-Martínez L., Carreón-Rodríguez A., González-Alzati M.E., Morales C., Charli J.L., Joseph-Bravo P. Dexamethasone rapidly regulates TRH mRNA levels in hypothalamic cell cultures: interactions with the cAMP pathway. Neuroendocrinology. 68:1998;345-354.
27. Pu L.P., Ma W., Barker J.L., Loh Y.P. Differential coexpression of genes encoding prothyrotropin-releasing hormone (Pro-TRH) and prohormone convertases (PC1 and PC2) in rat brain neurons: implications for differential processing of pro-TRH. Endocrinology. 137:1996;1233-1241.
28. Sánchez E., Charli J.L., Morales C., Corkidi G., Seidah N., Joseph-Bravo P., Uribe R.M. Expression of the proprotein convertases PC1 and PC2 mRNAs in TRH neurons of the rat paraventricular nucleus of hypothalamus. Brain Res. 761:1997;77-86.
29. Sanes J.R. Extracellular matrix molecules that influence neural development. Ann. Rev. Neurosci. 12:1989;491-516.
30. Schaner P., Todd R.B., Seidah N.G., Nillni E.A. Processing of prothyrotropin-releasing hormone by the family of prohormone convertases. J. Biol. Chem. 272:1997;19958-19968.
31. Sephel G.C., Tashiro K.-I., Sasaki M., Greatorex D., Martin G.R., Yamada Y., Kleinman H.K. Laminin A chain synthetic peptide which supports neurite outgrowth. Biochem. Biophys. Res. Commun. 162:1989;821-829.
32. Vindrola O., Chervin A., Vitale M., Mella A.N., Aloyz R., Basso A. Elevated proenkephalin-derived peptide levels in ACTH-producing adenomas. Endocrine. 8:1998;231-240.
33. Zheng M., Streck R.D., Scott R.E.M., Seidah N.G., Pintar J.E. The developmental expression in rat of proteases furin, PC1, PC2 and carboxypeptidase E: implications for early maturation of proteolytic processing capacity. J. Neurosci. 14:1994;4656-4673.