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Biology subjects

Monteiro, J.

Publications and source records attributed to Monteiro, J..

2 recordsLinked to original sources

Aridity and coexistence with vascular plants determine the dynamics of coastal dune bryophyte communities

The bryophyte communities of Atlantic coastal dunes help stabilising these habitats by promoting nutrient fixation, contributing to soil consolidation and enhancing water retention. Because of climate change and sea level rise, negative impacts on this dune vegetation have already been recorded, including habitat loss, shifts in species distribution and the spread of invasive bryophyte species. Moreover, in this stressful environment, biotic interactions may play a key in shaping plant diversity at these scales. We characterised coastal dune vegetation in 32 sampling sites along a latitudinal aridity gradient across the western Iberian Atlantic. We aimed to assess the potential interactions among moss species and between mosses and vascular plants, and analyse their relationship with abiotic factors to explain the community dynamics of dune bryophytes, and forecast how these communities may respond to climate change. Our results showed that the moss community is mainly influenced by aridity and temperature, with biotic interactions playing a minor, yet significant, role. As aridity increases, moss cover in these dune environments will decrease, and interactions with other plants are unlikely to compensate for this decline, thus in a climate change scenario we expect a decrease in coastal bryophyte community as well as the ecosystem services they provide; simultaneously the spread of the alien moss species Campylopus introflexus, linked to lower aridity, may also slow down. Consequently, the changing climate will shift optimal conditions for moss species to higher latitudes, pushing competition further north

ecology↗

Molecular mechanisms of coronary artery disease risk at the PDGFD locus

Platelet derived growth factor (PDGF) signaling has been extensively studied in the context of vascular disease, but the genetics of this pathway remain to be established. Genome wide association studies (GWAS) for coronary artery disease (CAD) have identified a risk locus at 11q22.3, and we have verified with fine mapping approaches that the regulatory variant rs2019090 and PDGFD represent the functional variant and putative functional gene. Further, FOXC1/C2 transcription factor (TF) binding at rs2019090 was found to promote PDGFD transcription through the CAD promoting allele. Employing a constitutive Pdgfd knockout allele along with SMC lineage tracing in a male atherosclerosis mouse model we mapped single cell transcriptomic, cell state, and lesion anatomical changes associated with gene loss. These studies revealed that Pdgfd promotes expansion, migration, and transition of SMC lineage cells to the chondromyocyte phenotype and vascular calcification. This is in contrast to protective CAD genes TCF21, ZEB2, and SMAD3 which we have shown to promote the fibroblast-like cell transition or perturb the pattern or extent of transition to the chondromyocyte phenotype. Further, Pdgfd expressing fibroblasts and pericytes exhibited greater expression of chemokines and leukocyte adhesion molecules, consistent with observed increased macrophage recruitment to the plaque. Despite these changes there was no effect of Pdgfd deletion on SMC contribution to the fibrous cap or overall lesion burden. These findings suggest that PDGFD mediates CAD risk through promoting SMC expansion and migration, in conjunction with deleterious phenotypic changes, and through promoting an inflammatory response that is primarily focused in the adventitia where it contributes to leukocyte trafficking to the diseased vessel wall.

genetics↗