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CX3CL1-CX3CR1 Axis: A New Player in Coeliac Disease Pathogenesis.
Fernández-Prieto, Marta; Fernández-Aceñero, María Jesús; López-Palacios, Natalia; Bodas, Andrés; Farrais, Sergio; Cuevas, David; Pascual, Virginia; Cerón-Nieto, M Ángeles; Horta-Herrera, Saúl; Espino-Paisán, Laura; Salazar, Isabel; Núñez, Concepción.
Afiliação
  • Fernández-Prieto M; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. martafp87@gmail.com.
  • Fernández-Aceñero MJ; Servicio de Anatomía Patológica, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. mariajesus.fernandez@salud.madrid.org.
  • López-Palacios N; Servicio de Aparato Digestivo, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. natalia.lopa@gmail.com.
  • Bodas A; Servicio de Pediatría, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. andresbpinedo@yahoo.es.
  • Farrais S; Servicio de Aparato Digestivo, Hospital Universitario Fundación Jiménez Díaz, 28040 Madrid, Spain. sfarraisv@quironsalud.es.
  • Cuevas D; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. david94.cg@gmail.com.
  • Pascual V; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. virginia.pascual.01@gmail.com.
  • Cerón-Nieto MÁ; Servicio de Anatomía Patológica, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. nines.ceron@gmail.com.
  • Horta-Herrera S; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. hortaherrera.saul@gmail.com.
  • Espino-Paisán L; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. lauraep80@gmail.com.
  • Salazar I; Departamento de Producción Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040 Madrid, Spain. isalazar@ucm.es.
  • Núñez C; Laboratorio de Investigación en Genética de enfermedades complejas, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain. conchita.npardo@gmail.com.
Nutrients ; 11(11)2019 Oct 23.
Article em En | MEDLINE | ID: mdl-31652730
ABSTRACT

BACKGROUND:

The CX3CL1-CX3CR1 axis has been related to numerous diseases. The aim of our study was to investigate its involvement in coeliac disease (CD) pathogenesis, particularly in the early phase of the disease.

METHODS:

We collected peripheral blood from CD patients and controls, enrolled in a 3-day gluten challenge, to study soluble CX3CL1, I-TAC and MIG by Luminex, CX3CL1 and CX3CR1 gene expression by qPCR, and CX3CR1 protein expression in monocytes and CD8+, CD4+ and γδ+ T cells, by flow cytometry. We also analysed the expression of the CX3CL1 and CX3CR1 mRNA and protein in the duodenal biopsies of CD patients with active and treated disease, and in non-CD control individuals, by qPCR and immunohistochemistry.

RESULTS:

After the gluten challenge, increased levels of CX3CL1, I-TAC and MIG proteins were observed in the peripheral blood of CD patients, with no changes in CX3CL1 mRNA, or CX3CR1 mRNA and protein. Regarding duodenal tissue, CX3CL1 was absent or barely present in the superficial and basal epithelium of CD patients, contrasting with the moderate to high levels present in controls.

CONCLUSIONS:

CX3CL1 seems to be involved in the appearance and progression of CD, and it appears to be a potential diagnostic biomarker. Its use as an alternative therapeutic target in CD deserves further research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença Celíaca / Regulação da Expressão Gênica / Quimiocina CX3CL1 / Receptor 1 de Quimiocina CX3C Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença Celíaca / Regulação da Expressão Gênica / Quimiocina CX3CL1 / Receptor 1 de Quimiocina CX3C Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article