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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 4

Computational predictions of interactions between MMP25-AS1 and its associated protein-coding gene MMP25.

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Computational predictions of interactions between MMP25-AS1 and its asso...
LncTar software predictions of the normalized binding free energy (ndG) for the complementary regions between MMP25-AS1 and MMP25 (A). Note the minimum ndG (blue box) is –0.2626. Screenshot taken from the UCSC Genome Browser shows the genomic locations of MMP25 mRNA, MMP25-AS1 isoforms, and the 3′UTR genomic overlap (red circle) between exons 1 and 2 of the MMP25-AS1 isoform 4 (794 bp) and exons 9 and 10 of MMP25 mRNA (B). Screenshot of the NCBI Gene database page showing all 10 isoforms of MMP25-AS1 and their sizes (C). The sizes represent the total exon length of each isoform. CLUSTALW sequence alignment of MMP25-AS1/MMP25 showing complementary interactions (D and E). Note the presence of a large (D) (374 bp) and small perfect complementary region (E) (133 bp) between MMP25 and MMP25-AS1. Representation of exonic regions (regions 1–5) on the MMP25-AS1 isoform ENST00000572574.5 (794 bp) and the binding sites of the 3 PCR primer pairs used to amplify the RM 794 bp isoform (F). Expression patterns of MMP25-AS1 and MMP25 in 19 different tissues obtained from fetuses with congenital diseases (G) (data obtained from NIH epigenomics program). FPKM, Fragment per kilobase of transcript per million fragments mapped.

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