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Biology subjects

Kaye, A.

Publications and source records attributed to Kaye, A..

2 recordsLinked to original sources

Proteome of human glioblastoma and meningioma tissue small extracellular vesicles

Small extracellular vesicles have gained attention in neuroscience due to their role in cell-to- cell communication and their potential diagnostic and therapeutic applications. Despite progress in the field, there remains a gap in our understanding of the composition and function of extracellular vesicles with regards to brain tumours. Previous studies have primarily evaluated extracellular vesicles obtained from patient fluids or cell culture medium, rather than directly from tumour tissue. Here we successfully isolated small extracellular vesicles from surgical tissue biopsies of glioblastomas or meningiomas, marking, marking the first report of in situ extracellular vesicle isolation from brain tumours. The protein content of the tumour tissue and their extracellular vesicles was characterized using tandem mass spectrometric proteomics, revealing proteins exclusively detected or enriched in extracellular vesicles relative to the tumour tissue. While our study confirmed proteins previously identified in glioblastoma and meningioma extracellular vesicles from various sources, it also identified novel proteins and pathways associated with extracellular vesicles from these tumour types. This study underscores the benefit of analysing in situ extracellular vesicles derived directly from brain tissue for insights into tumour biology and highlights the need for further research comparing extracellular vesicles from various types and grades of brain tumours.

biochemistry↗

Intermittent fasting induces rapid hepatocyte proliferation

Nutrient availability fluctuates in most natural populations, forcing organisms to undergo periods of fasting and re-feeding. It is unknown how dietary changes influence liver homeostasis. Here, we show that a switch from ad libitum feeding to intermittent fasting, IF, promotes rapid hepatocyte proliferation. Mechanistically, IF-induced hepatocyte proliferation is driven by the combined action of intestinally produced, systemic endocrine FGF15 and localized WNT signaling. Hepatocyte proliferation during periods of fasting and re-feeding re-establishes a constant liver-to-body-mass ratio, thus maintaining the hepatostat. This study provides the first example of dietary influence on adult hepatocyte proliferation and challenges the widely held view that liver tissue is mostly quiescent unless chemically or mechanically injured.

cell biology↗