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Macedo, M.

Publications and source records attributed to Macedo, M..

2 recordsLinked to original sources

Recurrent Hermaphroditism and Sex-Biased ABCDE Gene Expression Reveal Latent Floral Plasticity in the Pedunculate Oak Lineage (Q.robur s.l.)

Background and AimsThe development of unisexual flowers relies on the tight coordination of flower organ identity and sex determination. The genus Quercus is typically considered strictly monoecious, bearing fully segregated male and female flowers within the same individual tree. However, several reports of atypical flowering across the genus challenge this canonical view, suggesting that flowering in oaks may be more flexible than traditionally assumed. In this work, the dynamics of flower development in Quercus orocantabrica were examined to correlate contrasting floral morphologies with divergent molecular profiles. MethodsThe flowering phenology of Q. orocantabrica trees was closely monitored over several individuals and years, together with a detailed floral morphological analysis of male, female and atypical flowers. Key floral homeotic gene homologues were identified, and their expression assayed in the development of different flowers. Key ResultsRecurrent and widespread hermaphroditic flowering was detected in several Q. orocantabrica trees, frequently associated with unseasonal flowering events. Gene expression analysis of male, female and hermaphroditic flowers revealed a sex-biased expression of Q. orocantabrica B- and C-class genes, with the B-class gene QoPI in particular being tightly associated with the presence of fully-developed stamens. In addition, the expression of the C-class gene QoSHP contrasted with reports in other Fagaceae, highlighting a potential functional divergence of the C/D-class lineage within the family. ConclusionsThe results here depicted indicate that the dynamics of floral sex identity in oaks are more plastic than traditionally assumed, supporting a reinterpretation of oak reproductive biology based on a versatile and resilient framework responsive to different developmental contexts.

plant biology↗

Epidermal γδ T cells, CD8 T cells and macrophages are increased in number in alopecia areata and express BST2 as part of an interferon-driven antiviral gene signature

Alopecia areata is an autoimmune disorder affecting approximately 2% of the global population, characterized by immune-mediated disruption of hair follicle immune privilege and unpredictable hair loss. While CD4 and CD8 T cells are established drivers of pathogenesis, the roles of other immune cell populations remain incompletely defined. Here, we reaffirm the pathogenic role of CD8 T cells and identify a contribution of epidermal {gamma}{delta} T cells and macrophages to alopecia areata. Using publicly available single-cell RNA sequencing (scRNAseq) data from the skin of C3H/HeJ mice with alopecia areata, we demonstrate that epidermal {gamma}{delta} T cells upregulate genes associated with immune homeostasis, proliferation, and inflammation, including BST2, an interferon-stimulated antiviral protein. In vivo, epidermal {gamma}{delta} T cells and keratinocytes are increased in number, with BST2 expression enriched around hair follicles. BST2 is also expressed on CD8 T cells actively producing IFN-{gamma} and on CD11b+ macrophages with signatures of antiviral and complement system pathways. In human alopecia areata skin, BST2 expression is elevated in alopecia areata and downregulated following treatment with the JAK inhibitor tofacitinib. Together, these findings position BST2 as a marker of interferon-driven immune activation and highlight epidermal {gamma}{delta} T cells as a contributor to alopecia areata pathogenesis.

immunology↗