Ninjurin 1 asp110ala single nucleotide polymorphism is associated with protection in leprosy nerve damage

Abstract Leprosy is the major cause of non-traumatic neuropathy. Herein, we investigated the role of ninjurin 1, an adhesion molecule involved in nerve regeneration in leprosy. Our results demonstrated that M. leprae stimulates in vitro up-regulation of ninjurin mRNA in cultured Schwann and blood ce...

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Veröffentlicht in:Journal of neuroimmunology 2007-10, Vol.190 (1), p.131-138
Hauptverfasser: Cardoso, Cynthia Chester, Martinez, Alejandra Nóbrega, Guimarães, Pedro Edson Moreira, Mendes, Camila Teixeira, Pacheco, Antônio Guilherme, de Oliveira, Rosane Barbosa, Teles, Rosane Magda Brandão, Illarramendi, Ximena, Sampaio, Elizabeth Pereira, Sarno, Euzenir Nunes, Dias-Neto, Emmanuel, Moraes, Milton Ozório
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Sprache:eng
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Zusammenfassung:Abstract Leprosy is the major cause of non-traumatic neuropathy. Herein, we investigated the role of ninjurin 1, an adhesion molecule involved in nerve regeneration in leprosy. Our results demonstrated that M. leprae stimulates in vitro up-regulation of ninjurin mRNA in cultured Schwann and blood cells as well as in vivo mRNA and protein expression in leprosy nerve biopsies. A polymorphism (asp110ala) was investigated in a case–control study (1123 individuals) and no association was found with leprosy per se or with disseminated forms. Nevertheless, ala110 was associated with functional nerve impairment (OR = 2.42; p = 0.02 for ala/ala) and with lower mRNA levels. Our data suggests that asp110ala could be a valuable genetic marker of nerve damage in leprosy.
ISSN:0165-5728
1872-8421
DOI:10.1016/j.jneuroim.2007.07.015