scholarly journals Medroxyprogesterone Acetate (MPA) Enhances HIV-1 Accumulation and Release in Primary Cervical Epithelial Cells by Inhibiting Lysosomal Activity

Pathogens ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1192
Author(s):  
Xiangxu Jia ◽  
Qiujia Shao ◽  
Ahsen R. Chaudhry ◽  
Ballington L. Kinlock ◽  
Michael G. Izban ◽  
...  

Medroxyprogesterone acetate (MPA) is one of the most widely used contraceptives in the world. Epidemiologic studies have uncovered a possible link between the use of MPA and an increased risk of HIV-1 transmission. However, the understanding of the mechanism is still limited. Our previous publication demonstrated that the lysosomal activity in human vaginal epithelial cells attenuated the trafficking of viral particles during HIV-1 transcytosis. In this study, we show that treating human primary cervical epithelial cells with MPA led to a reduction in lysosomal activity. This reduction caused an increase in the intracellular HIV-1 accumulation and, consequently, an increase in viral release. Our study uncovers a novel mechanism by which MPA enhances HIV-1 release in primary cervical epithelial cells, thus providing vital information for HIV intervention and prevention.

PLoS ONE ◽  
2014 ◽  
Vol 9 (5) ◽  
pp. e96760 ◽  
Author(s):  
Ballington L. Kinlock ◽  
Yudi Wang ◽  
Tiffany M. Turner ◽  
Chenliang Wang ◽  
Bindong Liu

2011 ◽  
Vol 65 (6) ◽  
pp. 569-577 ◽  
Author(s):  
Irina A. Zalenskaya ◽  
Orlando G. Cerocchi ◽  
Theresa Joseph ◽  
Melissa A. Donaghay ◽  
Suzanne D. Schriver ◽  
...  

Viruses ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 557 ◽  
Author(s):  
Yu Liu ◽  
Xi-Qiu Xu ◽  
Biao Zhang ◽  
Jun Gu ◽  
Feng-Zhen Meng ◽  
...  

The Bowman‒Birk inhibitor (BBI), a protease inhibitor derived from soybeans, has been extensively studied in anti-tumor and anti-inflammation research. We recently reported that BBI has an anti-HIV-1 property in primary human macrophages. Because HSV-2 infection plays a role in facilitating HIV-1 sexual transmission, we thus examined whether BBI has the ability to inhibit HSV-2 infection. We demonstrated that BBI could potently inhibit HSV-2 replication in human cervical epithelial cells (End1/E6E7). This BBI-mediated HSV-2 inhibition was partially through blocking HSV-2-mediated activation of NF-κB and p38 MAPK pathways. In addition, BBI could activate the JAK/STAT pathway and enhance the expression of several antiviral interferon-stimulated genes (ISGs). Furthermore, BBI treatment of End1/E6E7 cells upregulated the expression of tight junction proteins and reduced HSV-2-mediated cellular ubiquitinated proteins’ degradation through suppressing the ubiquitin‒proteasome system. These observations indicate that BBI may have therapeutic potential for the prevention and treatment of HSV-2 infections.


2014 ◽  
Vol 211 (11) ◽  
pp. 1745-1756 ◽  
Author(s):  
Victor H. Ferreira ◽  
Sara Dizzell ◽  
Aisha Nazli ◽  
Jessica K. Kafka ◽  
Kristen Mueller ◽  
...  

2013 ◽  
Vol 208 (11) ◽  
pp. 1756-1767 ◽  
Author(s):  
Amanda M. Micsenyi ◽  
Chati Zony ◽  
Raymond A. Alvarez ◽  
Natasha D. Durham ◽  
Benjamin K. Chen ◽  
...  

2014 ◽  
Vol 30 (S1) ◽  
pp. A53-A54
Author(s):  
Victor H. Ferreira ◽  
Aisha Nazli ◽  
Jessica K. Kafka ◽  
Kristen Mueller ◽  
Michel J. Tremblay ◽  
...  

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