Diminished adherence and/or ingestion of virulent Mycobacterium tuberculosis by monocyte-derived macrophages from patients with tuberculosis

ABSTRACT: The interaction between the macrophage and Mycobacterium tuberculosis is mediated by a variety of macrophage membrane-associated proteins. Complement receptors have been implicated in the adherence of M. tuberculosis to macrophages. In the present work, the adherence and/or ingestion of M....

Full description

Autores:
Zabaleta Blanquicet, Jovanny
Arias Pineda, Mauricio Alberto
Maya, José Roberto
García Moreno, Luis Fernado
Tipo de recurso:
Article of investigation
Fecha de publicación:
1998
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/39033
Acceso en línea:
https://hdl.handle.net/10495/39033
Palabra clave:
Adhesión Bacteriana
Bacterial Adhesion
Células Cultivadas
Cells, Cultured
Recuento de Colonia Microbiana
Colony Count, Microbial
Medio de Cultivo Libre de Suero
Culture Media, Serum-Free
Macrófagos
Macrophages
Mycobacterium tuberculosis
Tuberculosis - inmunología
Tuberculosis - immunology
Flow Cytometry
Citometría de Flujo
Proteínas Opsoninas - sangre
Opsonin Proteins - blood
https://id.nlm.nih.gov/mesh/D001422
https://id.nlm.nih.gov/mesh/D002478
https://id.nlm.nih.gov/mesh/D015169
https://id.nlm.nih.gov/mesh/D016895
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D008264
https://id.nlm.nih.gov/mesh/D009169
https://id.nlm.nih.gov/mesh/D009895
https://id.nlm.nih.gov/mesh/D014376
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:ABSTRACT: The interaction between the macrophage and Mycobacterium tuberculosis is mediated by a variety of macrophage membrane-associated proteins. Complement receptors have been implicated in the adherence of M. tuberculosis to macrophages. In the present work, the adherence and/or ingestion of M. tuberculosis H37Rv to human monocyte-derived macrophages (MDM) from patients with tuberculosis (TB) and healthy controls was measured by microscopical examination, [3H]uracil incorporation, and CFU. The adherence and/or ingestion was enhanced by fresh serum and inhibited by heat inactivation, EDTA treatment, and anti-CR1 and anti-CR3 antibodies. Comparison of MDM from TB patients and healthy controls showed that the former exhibited a significantly decreased capacity to adhere and/or ingest M. tuberculosis, as determined by the number of CFU and 3H incorporation. The expression of CR1 (CD35) and CR3 (CD11b/CD18) on MDM from TB patients and healthy controls, as determined by flow cytometry, did not show significant differences. These results suggest that the lower ingestion of M. tuberculosis by MDM from TB patients is not due to defects in complement receptors, and therefore, there might be other molecules involved in the adherence and/or ingestion process that render MDM from TB patients ingest less mycobacteria than those from healthy controls.