Pericytes derived from the retinal microvasculature undergo calcification in vitro
0301 basic medicine
Cells
610
Fluorescent Antibody Technique
Cell Count
Tritium
Electron
Calcification
03 medical and health sciences
Calcification, Physiologic
Cell Differentiation/physiology
Animals
Cells, Cultured
Microscopy
Cultured
Histocytochemistry
Microcirculation
Retinal Vessels
Videotape Recording
600
Cell Differentiation
Thymidine/metabolism
Retinal Vessels/cytology
Microscopy, Electron
Cattle
Physiologic/physiology
Electron Probe Microanalysis
Thymidine
DOI:
10.1242/jcs.97.3.449
Publication Date:
2021-04-26T21:20:29Z
AUTHORS (5)
ABSTRACT
Pericytes isolated from the bovine retinal microvasculature retain characteristic features of their in vivo counterparts, such as presence glycogen deposits, long filamentous processes, prominent microfilament bundles and ability to display two distinct reversible phenotypes. Time-lapse video-microscopy demonstrated that pericytes tend overlap aggregate, even sparse cultures. After reaching confluence, they form multilayered areas retract away each other, resulting formation multicellular nodules. These nodules increase size cellularity by going through repeated 5- 6-h cycles anchoring, spreading, cell proliferation retraction. Alkaline phosphatase was not detected at subconfluent or confluent densities, but this enzyme expressed high density, multilayers synthesise deposit an extracellular matrix all stages vitro development, including nodule formation. The within contains cross-striated collagen fibres vesicles. Needle-like crystals hydroxyapatite appear be deposited matrix, thus leading massive calcification nodule. Calcification, assessed electron microscopy, histochemical staining X-ray microprobe analysis, occurred on plastic substrate absence disodium-beta-glycerophosphate. addition compound 5 10 mM use a substratum (rather than plastic), brought forward process 3-6 days. Our results suggest may differentiate along osteogenic pathway.
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