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MYCOBACTERIUM TUBERCULOSIS STRAIN H37RV INFECTION TOWARDS MATRIX METALLOPROTEINASE (MMP)-2 IN BRAIN
Author(s) -
Kevin Hartono,
Prasetyo Adi,
Dwi Yuni Nur Hidayati
Publication year - 2017
Publication title -
mnj (malang neurology journal)
Language(s) - English
Resource type - Journals
eISSN - 2442-5001
pISSN - 2407-6724
DOI - 10.21776/ub.mnj.2017.003.02.2
Subject(s) - matrix metalloproteinase , immune system , inflammation , microglia , immunohistochemistry , pathology , tumor necrosis factor alpha , biology , matrix (chemical analysis) , secretion , tuberculosis , necrosis , lesion , immunology , medicine , chemistry , endocrinology , biochemistry , chromatography
Background. Tuberculous infection in brain can cause microglia to secrete inflammatory factors like  Tumor Necrosis Factor alpha (TNF-α) and Interleukin 1 beta (IL-1β) which will be shown as body immune  respons. Those inflammatory factors eventually can trigger microglia to secrete Matrix Metalloproteinase- 2 (MMP-2) which will regenerate necrotic or apoptosis cells because of inflammation process. MMP-2 has  been proven to have important role in brain tuberculous infection. Objective. To ascertain MMP-2 expression in mus musculus brain tissue with no infection, infection for 8 weeks, and infection for 16 weeks. Methods. This research used semiquantitative method to compare MMP-2 expression in 3 samples group. Observation of MMP-2 expression in mus musculus brain tissue were made by using immunohistochemistry colouration method which then would be observed in microscope with 400x magnification. Brain cell which express MMP-2 will become brown in cell nucleus, cytoplasm, and wall. Results. The result which had be obtained was overtime reduction of MMP-2 expression. Conclusion. MMP-2 expression didn’t decrease after 8 weeks time of infection.

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