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Biology subjects

Arthur, P.

Publications and source records attributed to Arthur, P..

2 recordsLinked to original sources

Paradoxical energetics in the polar diatom Fragilariopsis cylindrus exposed to extreme low light

In the Arctic Ocean, diatoms initiate blooms under sea ice at extreme low-light levels, yet the limits and mechanisms behind this capability remain unknown. We investigated the steady-state physiological and molecular responses of the polar diatom Fragilariopsis cylindrus across a light gradient (0.1 to 30 {micro}mol photons m-2 s-1), representative of under-ice winter to early spring conditions, and reveals distinct strategies to cope with low light at both ends of this range. While cells optimize photon capture efficiency between 3 and 15 {micro}mol photons m-2 s-1 relative to 30 {micro}mol photons m-2 s-1, this strategy collapses below 1 {micro}mol photons m-2 s-1. In this dim-light regime, cells activate non-photochemical quenching and a sustained xanthophyll cycle, which indicates a paradoxical requirement for energy dissipation despite extreme photon scarcity. While cell division arrests at 0.18 {micro}mol photons m-2 s-1, photosynthetic electron transport seems to remain possible down to 0.1 {micro}mol photons m-2 s-1, which suggests an uncoupling between photosynthesis and biomass accumulation. Crucially, this low-light regime occurs without the consumption of reserves and represents a physiological state distinct from metabolic hypometabolism in prolonged darkness. We propose that this dim-light physiological state arises when residual light absorption exceeds the energetic requirements for cellular maintenance in the absence of division. The result is a regulated imbalance dissipated through heat and carbon excretion. This mechanism allows polar diatoms to maintain a primed photosynthetic metabolism to facilitate rapid growth recovery upon the return of light after the winter solstice.

plant biology↗

Biophysical, Molecular and Proteomic profiling of Human Retinal Organoids derived Exosomes

Extracellular vesicles (EVs) are phospholipid bilayer-bound particles released by cells that play a role in cell-cell communication, signal transduction, and extracellular matrix remodeling. There is a growing interest in EVs for ocular applications as therapeutics, biomarkers, and drug delivery vehicles. EVs secreted from mesenchymal stem cells (MSCs) have shown to provide therapeutic benefits in ocular conditions. However, very little is known about the properties of bioreactors cultured-3D human retinal organoids secreted EVs. This study provides a comprehensive morphological, nanomechanical, molecular, and proteomic characterization of retinal organoid EVs and compares it with human umbilical cord (hUC) MSCs. Nanoparticle tracking analysis indicated the average size of EV as 100-250 nm. Atomic force microscopy showed that retinal organoid EVs are softer and rougher than the hUCMSC EVs. Gene expression analysis by qPCR showed a high expression of exosome biogenesis genes in late retinal organoids derived EVs (>120 days). Immunoblot analysis showed highly expressed exosomal markers Alix, CD63, Flotillin-2, HRS and Hsp70 in late retinal organoids compared to early retinal organoids EVs (<120 days). Protein profiling of retinal organoid EVs displayed a higher differential expression of retinal function-related proteins and EV biogenesis/marker proteins than hUCMSC EVs, implicating that the use of retinal organoid EVs may have a superior therapeutic effect on retinal disorders. This study adds supplementary knowledge on the properties of EVs secreted by retinal organoids and suggests their potential use in the diagnostic and therapeutic treatments for ocular diseases.

bioengineering↗