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Invasion of human microvascular endothelial cells by Mycobacterium leprae through Mce1A protein.
Idris, Irfan; Abdurrahman, Ahmad Haykal; Aftitah, Vienza Beby; Fadlitha, Viesta Beby; Sato, Naoya; Fujimura, Takao; Takimoto, Hiroaki.
Afiliação
  • Idris I; Hasanuddin University Medical Research Center, Makassar, Indonesia.
  • Abdurrahman AH; Departments of, Departments of, Dermatology, Kitasato University Graduate School of Medical Science, Sagamihara, Japan.
  • Fatulrachman; Hasanuddin University Medical Research Center, Makassar, Indonesia.
  • Aftitah VB; Departments of, Departments of, Dermatology, Kitasato University Graduate School of Medical Science, Sagamihara, Japan.
  • Fadlitha VB; Departments of, Departments of, Dermatology, Kitasato University Graduate School of Medical Science, Sagamihara, Japan.
  • Sato N; Cellular Immunology, Kitasato University Graduate School of Medical Science, Sagamihara, Japan.
  • Fujimura T; Departments of, Departments of, Dermatology, Kitasato University Graduate School of Medical Science, Sagamihara, Japan.
  • Takimoto H; Department of Dermatology, Toshiba Rinkan Hospital, Sagamihara, Japan.
J Dermatol ; 46(10): 853-858, 2019 Oct.
Article em En | MEDLINE | ID: mdl-31432529
ABSTRACT
In patients with lepromatous leprosy, Mycobacterium leprae is often observed inside the human microvascular endothelial cells (HMVEC) surrounding Schwann cells (SC) at the site of lesions in the peripheral nerves. Based on this observation, it is considered that the nasal mucous may be the invasion pathway for M. leprae and HMVEC serve as an important reservoir for the bacteria before they invade SC. In light of previous research which revealed that Mce1A protein mediates bacterial invasion into nasal epithelial cells and HMVEC, we conducted a study to determine whether the invasion of M. leprae into HMVEC can be suppressed by blocking the Mce1A protein. In this study, we analyzed bacterial invasive activity by adding recombinant Escherichia coli, which express the active region (InvX72 a.a.) of Mce1A protein on their external membrane, into cultured HMVEC, using the adhesin involved in the diffuse adherence mechanism. The number of bacteria that invaded into the cells was then measured by a colony counting method. The active region of Mce1A was divided into four sections, and hyperimmune antisera was prepared for each section for analyzing the inhibitory effect against invasion. The invasive activity was suppressed by antibodies against InvX regions 1-24 a.a., 25-46 a.a. and 58-72 a.a. This suggests that the InvX regions 1-24 a.a., 25-46 a.a. and 58-72 a.a. of Mce1A protein play an important role in the invasion of M. leprae into HMVEC and that it may be possible to suppress entry of M. leprae in HMVEC with antibodies against these regions.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Células Endoteliais / Hanseníase / Anticorpos Antibacterianos / Mycobacterium leprae Limite: Animals / Humans Idioma: En Revista: J Dermatol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Células Endoteliais / Hanseníase / Anticorpos Antibacterianos / Mycobacterium leprae Limite: Animals / Humans Idioma: En Revista: J Dermatol Ano de publicação: 2019 Tipo de documento: Article