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Biology subjects

Cimadomo, D.

Publications and source records attributed to Cimadomo, D..

2 recordsLinked to original sources

NanoCT-confocal mapping of mouse ovaries reveals lifespan-persistent symmetric organizational rules of primary-to-preovulatory follicles

Mammalian ovaries are organized into follicles integrated with the surrounding tissue, collectively shaping an architecture continuously remodeled through cycles of growth and elimination. Combining nano-Computed Tomography with 3D digital modeling, we deciphered spatial rules governing follicle organization in the mouse ovary across lifespan. We find that primary to preovulatory follicles adopt a quantitatively symmetric arrangement along the anterior-posterior and dorsal-ventral axes, established during prepuberty before secondary follicle vascularization and preserved through adulthood and aging, regardless of follicle health or atresia. A novel nanoCT-confocal pipeline revealed that follicles enclosing oocytes with transcriptionally-active or transcriptionally-inactive chromatin states follow divergent fates of growth, atresia, or developmental competence, yet retaining a symmetric distribution. Mathematical modeling of follicle growth and elimination from prepuberty to adulthood identified transition rates between follicle stages that support gonadal symmetry. These findings suggest an evolutionarily optimized developmental program ensuring follicle recruitment and high ovulatory output, a hallmark of polytocous species.

developmental biology↗

The imprinted Mir483 is a growth suppressor and metabolic regulator functioning through IGF1

Mir483 is a conserved and highly expressed microRNA in placental mammals, embedded within the Igf2 gene. Here, we uncover the control mechanisms and physiological functions of Mir483 in vivo, by generating constitutive loss-of-function and over-expressing mice. Mir483 expression is imprinted and dependent on the Igf2 promoters and Igf2/H19 imprinting control region. Over-expression of Mir483 causes severe mid-gestation fetal, but not placental, growth restriction, and late lethality. Fetal death is prevented by restoring Mir483 to endogenous levels using an inducible transgenic system. Continuous postnatal Mir483 over-expression induces growth stunting, elevated hepatic lipid content, increased adiposity, reduced local and systemic IGF1 levels and increased GH. The growth phenotypes are rescued by IGF1 infusion. Our findings provide evidence for a novel functional antagonism between a growth-suppressor microRNA and its growth-promoter host gene, and suggest that Mir483 evolved to limit excessive tissue growth through repression of IGF ligand signalling.

developmental biology↗