Vitamin D, cell death pathways, and tuberculosis

Manik Retno Wahyunitisari and Ni Made Mertaniasih and Muhammad Amin and Wayan T. Artama and Eko Budi Koendhori (2017) Vitamin D, cell death pathways, and tuberculosis. International Journal of Mycobacteriology, 6 (1). pp. 349-355. ISSN 2212-5531

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Official URL: http://www.ijmyco.org/article.asp?issn=2212-5531;y...

Abstract

Background: Mycobacterium tuberculosis induces cellular necrosis that could promote spread of infection. The aim of this study is to analyze the effects of Vitamin D3 supplementation to improve the effectiveness of 2nd-line anti-tuberculosis (TB) drug therapy, especially in relation with cell death pathways. Methods: Mus musculus C3HeB/FeJ was randomly divided into four groups containing eight animals each. The 1st group (G1), consisting of mice that were intratracheally infected with multidrug-resistant strain of M. tuberculosis and sacrificed on 2-week postinfection to confirm successful infection. (G2) was a group of TB mice without therapy. Then, (G3) was a group of mice with the 2nd-line anti-TB therapy. The last group (G4) was a group of mice receiving not only the 2nd-line anti-TB therapy but also daily oral Vitamin D3 supplementation. Immunohistochemistry was used to measure expression of nuclear Vitamin D receptor, apoptosis marker cleaved caspase-3, cathelin-related antimicrobial peptide (CRAMP) and LC3B autophagy markers, necrosis marker RIPK3, and collagenase matrix metalloproteinase-1 (MMP1). The number of bacteria in the lung was calculated by colony forming units. The partial least square structural equation modeling with SmartPLS 3.2.6 software was used to analyze structural models among the variables. Results: Supplementation of Vitamin D3 on the 2nd-line anti-TB therapy increases Vitamin D3 receptor, CRAMP, LC3B, caspase-3 (P = 0.026, P = 0.000, P= 0.001), presses MMP1, and the number of bacteria (P = 0.010 and P= 0.000, respectively). The structural equation modeling analysis shows that increasing autophagy pathways reduces necrosis by lowering MMP1, whereas apoptosis reduces necrosis by decreasing the number of bacteria (each with indirect effects − 0.543 and − 0.544). Conclusion: A comprehensive analysis with the partial least square structural equation modeling shows decreasing necrosis requires increasing autophagy and apoptosis.

Item Type: Article
Uncontrolled Keywords: Apoptosis, autophagy, matrix metalloproteinase-1, multidrug-resistant-tuberculosis, necrosis, Vitamin D3
Subjects: R Medicine > R Medicine (General)
R Medicine > RZ Other systems of medicine
Divisions: 01. Fakultas Kedokteran > Mikrobiologi Klinik
Creators:
CreatorsNIM
Manik Retno WahyunitisariNIDN0021056602
Ni Made MertaniasihNIDN0007035703
Muhammad AminNIDN8804680018
Wayan T. ArtamaUNSPECIFIED
Eko Budi KoendhoriNIDN0004096406
Depositing User: arys fk
Date Deposited: 13 Jan 2020 07:21
Last Modified: 13 Jan 2020 07:21
URI: http://repository.unair.ac.id/id/eprint/93442
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