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Altered processing of the neurotensin/neuromedin N precursor in PC2 knock down mice: a biochemical and immunohistochemical study

2002; Wiley; Volume: 82; Issue: 4 Linguagem: Inglês

10.1046/j.1471-4159.2002.00988.x

1471-4159

Pierre Villeneuve, Sylvain Féliciangéli, Gilles Croissandeau, Nabil G. Seidah, Majambu Mbikay, Patrick Kitabgi, Alain Beaudet,

Hypothalamic control of reproductive hormones

Abstract Neurotensin (NT) and neuromedin N (NN) are generated by endoproteolytic cleavage of a common precursor molecule, pro‐NT/NN. To gain insight into the role of prohormone convertases PC1, PC2, and PC7 in this process, we investigated the maturation of pro‐NT/NN in the brain of PC7 (PC7−/–), PC2 (PC2–/–), and/or PC1 (PC1+/– and PC2–/–; PC1+/–) knock down mice. Inactivation of the PC7 gene was without effect, suggesting that this convertase is not involved in the processing of pro‐NT/NN. By contrast, there was a 15% decrease in NT and a 50% decrease in NN levels, as measured by radioimmunoassay, in whole brain extracts from PC2 null as compared with wild type mice. Using immunohistochemistry, we found that this decrease in pro‐NT/NN maturation products was uneven and that it was most pronounced in the medial preoptic area, lateral hypothalamus, and paraventricular hypothalamic nuclei. These results suggest that PC2 plays a critical role in the processing of pro‐NT/NN in mouse brain and that its deficiency may be compensated to a regionally variable extent by other convertases. Previous data have suggested that PC1 might be subserving this role. However, there was no change in the maturation of pro‐NT/NN in the brain of mice in which the PC1 gene had been partially inactivated, implying that complete PC1 knock down may be required for loss of function.