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Gijbels, M.

Publications and source records attributed to Gijbels, M..

3 recordsLinked to original sources

Atherosclerotic plaque iron accumulation characterizes a distinct phase of intra-plaque hemorrhage and is associated with inflammation and remodeling

Intraplaque haemorrhage (IPH) is a hallmark of advanced atherosclerosis and a major risk factor for ischemic stroke and myocardial infarction. Current IPH classification focusses on extravascular erythrocyte presence as a proxy of acute bleeding, where iron detection generally indicates older haemorrhages. While often used interchangeably, a comprehensive analysis of transcriptional and metabolic context and impact of iron and erythrocyte deposition on the plaque is still lacking. Here, we investigate iron as a late-stage IPH hallmark in human atherosclerotic plaques. We analysed erythrocyte-rich, iron-rich, and non-IPH regions in human carotid endarterectomy plaques by re-analysing a published transcriptomic dataset of 43 patient samples. In addition, we performed histological and immune phenotyping to define plaque traits associated with iron versus erythrocyte accumulation. Finally, we performed spatial metabolic profiling to functionally define iron-rich regions. Although iron and erythrocyte deposits frequently co-localised, both co-related with different histological traits. While iron- and erythrocyte-rich regions shared transcriptomic features of advanced plaques compared with non-IPH regions, direct comparison showed differences in gene expression profiles. Iron deposition was associated with increased myeloid cell accumulation and a unique spatial metabolic signature distinct from erythrocyte-rich and non-IPH regions. While sharing many characteristics with IPH plaques, the molecular, cellular and metabolic landscape of iron-rich regions is marked by features of plaque remodelling and repair. This makes iron deposition a unique hallmark of late-stage IPH, extending the current erythrocyte-based definition of IPH.

pathology↗

MicroRNA-26b protects against MASH development and can be efficiently targeted with lipid nanoparticles.

Background & AimsThe prevalence of metabolic dysfunction-associated steatohepatitis (MASH) is increasing, urging more research into the underlying mechanisms. MicroRNA-26b (miR-26b) might play a role in several MASH-related pathways. Therefore, we aimed to determine the role of miR-26b in MASH and its therapeutic potential using miR-26b mimic-loaded lipid nanoparticles (LNPs). MethodsApoe-/-Mir26b-/-, Apoe-/-LysMcreMir26bfl/fl mice, and respective controls were fed a western-type diet to induce MASH. Plasma and liver samples were characterized regarding lipid metabolism, hepatic inflammation, and fibrosis. Additionally, miR-26b mimic-loaded LNPs were injected in Apoe-/-Mir26b-/- mice to rescue the phenotype and key results were validated in human precision-cut liver slices. Finally, kinase profiling was used to elucidate underlying mechanisms. ResultsApoe-/-Mir26b-/- mice showed increased hepatic lipid levels, coinciding with increased expression of scavenger receptor a and platelet glycoprotein 4. Similar effects were found in mice lacking myeloid-specific miR-26b. Additionally, hepatic TNF and IL-6 levels and amount of infiltrated macrophages were increased in Apoe-/- Mir26b-/- mice. Moreover, Tgfb expression was increased by the miR-26b deficiency, leading to more hepatic fibrosis. A murine treatment model with miR-26b mimic-loaded LNPs reduced hepatic lipids, rescuing the observed phenotype. Kinase profiling identified increased inflammatory signaling upon miR-26b deficiency, which was rescued by LNP treatment. Finally, miR-26b mimic-loaded LNPs also reduced inflammation in human precision-cut liver slices. ConclusionsOverall, our study demonstrates that the detrimental effects of miR-26b deficiency in MASH can be rescued by LNP treatment. This novel discovery leads to more insight into MASH development, opening doors to potential new treatment options using LNP technology. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=100 SRC="FIGDIR/small/580792v2_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@b8b5b8org.highwire.dtl.DTLVardef@a26333org.highwire.dtl.DTLVardef@11ed2a0org.highwire.dtl.DTLVardef@963208_HPS_FORMAT_FIGEXP M_FIG C_FIG

pathology↗

Crucial role of Juvenile Hormone receptor components Methoprene-tolerant and Taiman in sexual maturation of adult male desert locusts (Schistocerca gregaria)

The desert locust, Schistocerca gregaria, is an infamous migrating insect, generally considered to be one of the most dangerous pest species worldwide. In an area that encompasses one fifth of the Earths land surface, desert locust swarms can devastate the agricultural production. Consequently, they pose a serious threat to food security and can have a dramatic socio-economic impact. Currently (in 2020), large parts of East Africa, Southwest and South Asia are experiencing the worst desert locust plague in many decades. Exceptionally high rainfall in different regions has caused the favorable environmental conditions for very successful reproduction and population growth. To better understand the molecular mechanisms responsible for this remarkable reproductive capacity, as well as to fill existing knowledge gaps regarding the regulation of male reproductive physiology, we decided to investigate the role of the methoprene-tolerant (Scg-Met) and taiman (Scg-Tai) genes in adult male desert locusts. Methoprene-tolerant and Taiman belong to the basic helix-loop-helix/Per-Arnt-Sim (bHLH/PAS) family of transcription factors and form a complex that is responsible for transducing the Juvenile Hormone (JH) signal. So far, in vivo research has mainly focused on the role of these JH receptor components in post-embryonic development, as well as in the reproductive physiology of adult female insects. In the current study, we show that silencing these components by RNA interference strongly inhibits sexual maturation of gregarious desert locust males, thereby severely disrupting reproduction. This observation is evidenced by the absence of a yellow colored cuticle, the significant reduction in the relative weight of the testes, the inability to show mating behavior, and the drastically reduced phenylacetonitrile (PAN) pheromone levels of the treated males. In addition, we also observed significant reductions of the relative weight, as well as the relative protein content, of the male accessory glands in Scg-Met knockdown locusts. Interestingly, in these animals the size of the corpora allata (CA), the endocrine glands where JH is synthesized, was significantly increased, and a significant rise was observed in the relative transcript levels of JH acid methyltransferase (JHAMT), a rate-limiting enzyme in the JH biosynthesis pathway. Moreover, other endocrine pathways also appeared to be affected by the knockdown, as evidenced by significant changes in the levels of the transcripts coding for the insulin-related peptide and for two neuroparsins in the fat body. Our results demonstrate that JH signaling pathway components play a crucial role in male reproductive physiology. Since they are crucial for a successful reproduction, they may hold great potential as candidate targets for the design of novel strategies for locust population management. Significance statementDesert locusts can form devastating swarms that threaten the livelihood in many of the worlds poorest countries, as demonstrated by the plagues in East Africa, Southwest and South Asia that are currently covered in the news worldwide. Control of this migratory pest mainly relies on the large-scale use of neurotoxic insecticides, also affecting non-target organisms in their already fragile habitats. Therefore, the identification of novel molecular targets for the design of more sustainable and more selective pest management techniques remains of crucial importance. Potential candidate targets in this respect are pathway components that transduce signals of typical insect hormones, such as ecdysteroids and juvenile hormones. By focusing in our current study on the JH receptor components, we showed that the reproductive capacities of desert locust males can be severely inhibited in an early stage, resulting in individuals that display no mating behavior, do not produce an important pheromone and do not show the characteristic yellow color of sexually mature gregarious males. Specifically targeting molecular components of the JH signaling pathway in future, more biorational control strategies could therefore be a very successful way by which expansion of these devastating plagues might be prevented.

molecular biology↗