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Biology subjects

Kostanjevec, K.

Publications and source records attributed to Kostanjevec, K..

2 recordsLinked to original sources

Long-term iododeoxyuridine labelling analysis finds no evidence of ovarian germline stem cell activity in adult or ageing mice

The purpose of this study was to determine whether ovarian germline stem cells or any adult mitotic cell type contribute to the adult oocyte pool in vivo from early adult through to aging mice. Long-term thymidine analogue labelling assays using iododeoxyuridine (IdU) were performed to identify mitotic cells and their descendants by immunohistochemistry for IdU and germline markers Ddx4 and Oct4. C57BL/6 mice at 10 weeks, 5 months and 12 months old were given IdU for 21-30 days through their drinking water to label all dividing cells, followed by washout periods of 0-10 weeks. Over 60,000 ovarian somatic cells and oocytes were scored in 111 ovaries. No double labelling of IdU with germline stem cell markers was found in oocytes at any stage of maturity, in mice at any age. In contrast, IdU exposure during embryogenesis resulted in large numbers of labelled oocytes in postnatal mice, as expected. We were therefore unable to confirm mitotic activity in stem cells or any other progenitor replenishing the oocyte pool in C57BL/6 mice. There is no evidence that quiescent stem cells are activated when the oocyte pool is depleted by age.

cell biology↗

Spiral-eyes: A soft active matter model of in vivo corneal epithelial cell migration

The mammalian cornea constantly regenerates its outer epithelial layer. Cells lost by abrasion are replaced by division of both corneal epithelial cells and stem cell populations around the corneal periphery, the limbus. Limbal-derived epithelial cells migrate into the cornea, maintaining equal rates of cell loss and replacement (the XYZ hypothesis). This process produces a striking stable spiral cell motion pattern across the corneal surface, with a central vortex. Here, we show that this spiral pattern can be explained by the interplay of limbus position, cell division, extrusion, and collective cell migration along the curved corneal surface. Using dissected LacZ mosaic murine corneas, we inferred the surface flow field by following stripe edges, revealing a tightening spiral. To explain these flow fields, we developed a cell-level in silico model treating corneal epithelial cells as soft, self-propelled particles with density-dependent proliferation and extrusion rates, and noisy alignment of migration direction. Even without global guidance cues, the model predicted stripes and spirals closely recapitulating experiment. A complementary continuum description generalised the XYZ hypothesis. Spiral formation was robust to curvature changes, but not topology, and sensitive to limbal stem cells and flocking alignment, showing how swarm physics on curved surfaces can explain tissue-scale biological processes.

biophysics↗