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Cannabinoid enhancement of lncRNA MMP25-AS1/MMP25 interaction reduces neutrophil infiltration and intestinal epithelial injury in HIV/SIV infection
Lakmini S. Premadasa, Eunhee Lee, Marina McDew-White, Xavier Alvarez, Sahana Jayakumar, Binhua Ling, Chioma M. Okeoma, Siddappa N. Byrareddy, Smita Kulkarni, Mahesh Mohan
Lakmini S. Premadasa, Eunhee Lee, Marina McDew-White, Xavier Alvarez, Sahana Jayakumar, Binhua Ling, Chioma M. Okeoma, Siddappa N. Byrareddy, Smita Kulkarni, Mahesh Mohan
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Research Article AIDS/HIV

Cannabinoid enhancement of lncRNA MMP25-AS1/MMP25 interaction reduces neutrophil infiltration and intestinal epithelial injury in HIV/SIV infection

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Abstract

Intestinal epithelial barrier dysfunction, a hallmark of HIV/SIV infection, persists despite viral suppression by combination antiretroviral therapy (cART). Emerging evidence suggests a critical role for long noncoding RNAs (lncRNAs) in maintaining epithelial homeostasis. We simultaneously profiled lncRNA/mRNA expression exclusively in colonic epithelium (CE) of SIV-infected rhesus macaques (RMs) administered vehicle (VEH) or Δ-9-tetrahydrocannabinol (THC). Relative to controls, fewer lncRNAs were up- or downregulated in CE of THC/SIV compared with VEH/SIV RMs. Importantly, reciprocal expression of the natural antisense lncRNA MMP25-AS1 (up 2.3-fold) and its associated protein-coding gene MMP25 (attracts neutrophils by inactivating alpha-1 anti-trypsin/SERPINA1) (down 2.2-fold) was detected in CE of THC/SIV RMs. Computational analysis verified 2 perfectly matched complementary regions and an energetically stable (normalized binding free energy = –0.2626) MMP25-AS1/MMP25 duplex structure. MMP25-AS1 overexpression blocked IFN-γ–induced MMP25 mRNA and protein expression in vitro. Elevated MMP25 protein expression in CE of VEH/SIV but not THC/SIV RMs was associated with increased infiltration by myeloperoxidase/CD11b++ neutrophils (transendothelial migration) and epithelial CD47 (transepithelial migration) expression. Interestingly, THC administered in combination with cART increased MMP25-AS1 and reduced MMP25 mRNA/protein expression in jejunal epithelium of SIV-infected RMs. Our findings demonstrate that MMP25-AS1 is a potentially unique epigenetic regulator of MMP25 and that low-dose THC can reduce neutrophil infiltration and intestinal epithelial injury potentially by downregulating MMP25 expression through modulation of MMP25-AS1.

Authors

Lakmini S. Premadasa, Eunhee Lee, Marina McDew-White, Xavier Alvarez, Sahana Jayakumar, Binhua Ling, Chioma M. Okeoma, Siddappa N. Byrareddy, Smita Kulkarni, Mahesh Mohan

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Figure 7

Effect of THC and cART on MMP25-AS1 and MMP25 expression in JE of SIV-infected RMs.

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Effect of THC and cART on MMP25-AS1 and MMP25 expression in JE of SIV-in...
RT-qPCR quantitation of MMP25-AS1 lncRNA expression (A) and MMP25 mRNA expression (B) levels in VEH/SIV/cART (n = 8) and THC/SIV/cART (n = 8) RMs before (Pre-infection) (n = 10) and at 5 months after SIV infection. One-way ANOVA (GraphPad Prism) was used to analyze ΔCT values. A P value of <0.05 was considered significant. MMP25 protein expression in JE of VEH/SIV/cART (n = 5) and THC/SIV/cART (n = 5) RMs before (Pre-infection) (n = 5) and at 5 months after SIV infection (C). Whole jejunum tissue sections were immunostained with antibodies against MMP25 (green). Note the increased MMP25 expression in JE of VEH/SIV/cART compared with THC/SIV/cART and the preinfection time point. Whole jejunum tissue sections from VEH/SIV/cART-5MPI (n = 8) and VEH/preinfection (n = 8), and THC/SIV/cART-5MPI (n = 8) and THC/preinfection (n = 8), were immunostained with antibodies against MPO (red) and CD11b (green), and DAPI (blue) for nuclear staining (D). Note the presence of MPO/CD11b++ neutrophils (yellow) in the jejunum lamina propria. Representative immunofluorescence images were captured using a Zeiss confocal microscope at 20× original magnification. Scale bars: 50 μm. Quantifying MMP25 signal intensity, specifically in the JE excluding lamina propria cells, was performed using a freehand tool available in HALO (area quantification method). MPO/CD11b++ cells were quantified using the highplex FL method available in HALO. Differences in MMP25 signal intensity (E) and MPO/CD11b++ cell numbers (F) between groups were analyzed using 1-way ANOVA employing the Prism v9 (GraphPad Prism). A P value of <0.05 was considered significant. Data represent mean ± SEM.

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