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Interleukin-1 and histamine are essential for inducing nickel allergy in mice.
Bando, Kanan; Kuroishi, Toshinobu; Sugawara, Shunji; Endo, Yasuo.
Afiliación
  • Bando K; Division of Orthodontics and Dentofacial Orthopedics, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
  • Kuroishi T; Division of Oral Immunology, Department of Oral Biology, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
  • Sugawara S; Division of Oral Immunology, Department of Oral Biology, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
  • Endo Y; Division of Oral and Maxillofacial Surgery, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
Clin Exp Allergy ; 49(10): 1362-1373, 2019 10.
Article en En | MEDLINE | ID: mdl-31325186
BACKGROUND: We previously reported that (a) lipopolysaccharide (LPS) is a potent adjuvant for inducing Nickel (Ni) allergy in mice at both the sensitization and elicitation steps, (b) LPS induces Interleukin-1 (IL-1) and histidine decarboxylase (HDC, the histamine-forming enzyme), and IL-1 induces HDC, (c) Ni allergy is induced in mast cell-deficient, but not IL-1-deficient (IL-1-KO) or HDC-KO mice. OBJECTIVE: To examine the roles of IL-1 and HDC (or histamine) and their interrelationship during the establishment of Ni allergy. METHODS: Ni (NiCl2 ) 1 mmol/L containing IL-1ß and/or histamine was injected intraperitoneally (sensitization step). Ten days later, test substance(s) were intradermally injected into ear pinnas (elicitation step), and ear swelling was measured. RESULTS: In wild-type mice, Ni + LPS or Ni + IL-1ß injection at sensitization step followed by Ni alone at elicitation step induced Ni allergy. In IL-1-KO, injection of Ni + IL-1ß (but not Ni + histamine) was required at both sensitization and elicitation steps to induce Ni allergy. In HDC-KO, Ni + IL-1ß + histamine at sensitization step followed by Ni + histamine at elicitation step induced Ni allergy. In histamine H1 receptor-deficient mice, IL-1ß induced HDC, but was ineffective as an adjuvant for inducing Ni allergy. In wild-type mice, injection into ear pinnas of Ni 10 mmol/L alone or Ni 1 mmol/L + LPS induced IL-1ß, HDC and a prolonged swelling of ear pinnas. In non-sensitized mice, injection of IL-1ß by itself into ear pinnas in IL-1-KO mice induced prolonged ear swelling. Ni augmented IL-1 production (both IL-1α and IL-1ß) and HDC induction in wild-type mice sensitized to Ni. CONCLUSIONS: In mice: (a) for inducing Ni allergy, IL-1 is essential at both the sensitization and elicitation steps, and HDC induction is involved in the effect of IL-1, (b) stimulation of H1 receptor is also essential for inducing Ni allergy at both sensitization and elicitation steps, and (c) the 'sensitization to Ni' state may be a state where tissues are primed for augmented production of IL-1α and/or IL-1ß in response to Ni. (within 300 words, now 300).
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Receptores Histamínicos H1 / Histamina / Interleucina-1alfa / Interleucina-1beta / Hipersensibilidad / Níquel Límite: Animals Idioma: En Revista: Clin Exp Allergy Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Receptores Histamínicos H1 / Histamina / Interleucina-1alfa / Interleucina-1beta / Hipersensibilidad / Níquel Límite: Animals Idioma: En Revista: Clin Exp Allergy Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón