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Mitochondria-associated microRNAs in rat hippocampus following traumatic brain injury
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“and that these miRNAs display a mitochondria-to-cytoplasm compartmental shift following a severe TBI [30, 31].”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“We reported previously that several inflammatory-responsive miRNAs (e.g., miR-146a, miR-142-3p, and miR-142-5p) are preferentially associated with mitochondria isolated from rat hippocampus”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“Interestingly, we did not find any evidence supporting the inter-organelle shift of other miRNAs such as miR-107, or miR-155, although these cytosolic miRNAs have been shown to be altered in TBI [31, 72].”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“These include three miRNAs, miR-146a, miR-142-3p, and miR-142-5p, that were previously identified to be highly enriched in rat hippocampal mitochondria [30, 31], as well as several other miRNAs including miR-223 and two neuronal-enriched miRNAs, miR-124 and miR-107 [62].”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“More specifically, our previous study shows that miR-146a, miR-142-3p, miR-142-5p, and miR-223 are predominately expressed in microglia and astrocytes [31], which is in line with the functional role of these miRNAs.”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“Our prior studies showed that, relative to the cytosol, miR-146a, miR-142-3p, and miR-142-5p are highly enriched in mitochondria isolated from rat hippocampus and postulated the presence of an inter-organelle network for miRNA localization and trafficking [29, 31].”
From The Mitochondria-Associated ER Membranes Are Novel Subcellular Locations Enriched for Inflammatory-Responsive MicroRNAs (2020) · cites this paper as [31]
In the citing paper
“Previous microarray data (41) and data obtained from cell cultures (42) also pointed to an enriched expression of miR-146a in microglia compared to other CNS resident cells.”
From Absence of miRNA-146a Differentially Alters Microglia Function and Proteome (2020) · cites this paper as [42]
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Cites
The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments
Bustin, S. A., Benes, V., Garson, J. A., Hellemans, J., Huggett, J., Kubista, M., Mueller, R., Nolan, T., Pfaffl, M. W., Shipley, G. L., et al. (2009) · Clinical Chemistry · doi:10.1373/clinchem.2008.112797 · Cited by 16,303
A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing
Landgraf, P., Rusu, M., Sheridan, R., Sewer, A., Iovino, N., Aravin, A., Pfeffer, S., Rice, A., Kamphorst, A. O., Landthaler, M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.04.040 · Cited by 3,626
Gene silencing by microRNAs: contributions of translational repression and mRNA decay
Huntzinger, E., & Izaurralde, E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2936 · Cited by 2,339
Mitochondria: More Than Just a Powerhouse
McBride, H. M., Neuspiel, M., & Wasiak, S. (2006) · Current Biology · doi:10.1016/j.cub.2006.06.054 · Cited by 1,985
Requirement of bic/microRNA-155 for Normal Immune Function
Rodriguez, A., Vigorito, E., Clare, S., Warren, M. V., Couttet, P., Soond, D. R., van Dongen, S., Grocock, R. J., Das, P. P., Miska, E. A., et al. (2007) · Science · doi:10.1126/science.1139253 · Cited by 1,833
MicroRNAs and immunity: Novel players in the regulation of normal immune function and inflammation
Sonkoly, E., Ståhle, M., & Pivarcsi, A. (2008) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2008.01.005 · Cited by 523 · cited 3×
“The levels of miR-155 and miR-223, both of which play a role in several biological/ pathological processes including immunity, cancer, and inflammatory responses (Sonkoly et al., 2008; Quinn and O’Neill, 2011; Higgs and Slack, 2013; Vigorito et al., 2013; Seddiki et al., 2014; Taibi et al., 2014), were significantly e…”
BackgroundmiR‐155 as a multiple sclerosis–relevant regulator of myeloid cell polarization
Moore, C. S., Rao, V. T. S., Durafourt, B. A., Bedell, B. J., Ludwin, S. K., Bar‐Or, A., & Antel, J. P. (2013) · Annals of Neurology · doi:10.1002/ana.23967 · Cited by 219 · cited 1×
“MiR-155 is known to participate in the regulation of inflammatory responses (KurowskaStolarska et al., 2011; Moore et al., 2013), which also occur at early time points following TBI.”
BackgroundThe multiple roles of microRNA-155 in oncogenesis
Higgs, G., & Slack, F. (2013) · Journal of Clinical Bioinformatics · doi:10.1186/2043-9113-3-17 · Cited by 137 · cited 2×
“The levels of miR-155 and miR-223, both of which play a role in several biological/ pathological processes including immunity, cancer, and inflammatory responses (Sonkoly et al., 2008; Quinn and O’Neill, 2011; Higgs and Slack, 2013; Vigorito et al., 2013; Seddiki et al., 2014; Taibi et al., 2014), were significantly e…”
BackgroundExpression of miR-15/107 Family MicroRNAs in Human Tissues and Cultured Rat Brain Cells
Wang, W.-X., Danaher, R. J., Miller, C. S., Berger, J. R., Nubia, V. G., Wilfred, B. S., Neltner, J. H., Norris, C. M., & Nelson, P. T. (2014) · Genomics, Proteomics & Bioinformatics · doi:10.1016/j.gpb.2013.10.003 · Cited by 67
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Metadata
- Authors
- Wang, W.-X., Visavadiya, N. P., Pandya, J. D., Nelson, P. T., Sullivan, P. G., & Springer, J. E.
- Venue
- Experimental Neurology
- Publisher
- Elsevier BV
- Published
- 2015-03
- Volume
- 265
- Pages
- 84-93
- ISSN
- 0014-4886
- PMC
- PMC4346439
- Cited by
- 134
- References
- 9
- Language
- en
- Funders
- Morton Cure Paralysis Fund
- Cardinal Hill Rehabilitation Hospital
- National Center for Advancing Translational Sciences (UT1TR000117)
- National Institutes of Health (UL1TR000117)
- PHS (NS085830, AG042419)
- KSCHIRT
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