Calcium imaging in intact mouse acinar cells in acute pancreas tissue slices.

The physiology and pathophysiology of the exocrine pancreas are in close connection to changes in intra-cellular Ca2+ concentration. Most of our knowledge is based on in vitro experiments on acinar cells or acini enzymatically isolated from their surroundings, which can alter their structure, physio...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Marolt Urška
Paradiž Leitgeb Eva
Pohorec Viljem
Lipovšek Saška
Venglovecz Viktória
Gál Eleonóra
Ébert Attila
Menyhárt István
Potrč Stojan
Gosak Marko
Dolenšek Jurij
Stožer Andraž
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:PLOS ONE 17 No. 6
Tárgyszavak:
doi:10.1371/journal.pone.0268644

mtmt:32867137
Online Access:http://publicatio.bibl.u-szeged.hu/24498
Leíró adatok
Tartalmi kivonat:The physiology and pathophysiology of the exocrine pancreas are in close connection to changes in intra-cellular Ca2+ concentration. Most of our knowledge is based on in vitro experiments on acinar cells or acini enzymatically isolated from their surroundings, which can alter their structure, physiology, and limit our understanding. Due to these limitations, the acute pancreas tissue slice technique was introduced almost two decades ago as a complementary approach to assess the morphology and physiology of both the endocrine and exocrine pancreas in a more conserved in situ setting. In this study, we extend previous work to functional multicellular calcium imaging on acinar cells in tissue slices. The viability and morphological characteristics of acinar cells within the tissue slice were assessed using the LIVE/DEAD assay, transmission electron microscopy, and immunofluorescence imaging. The main aim of our study was to characterize the responses of acinar cells to stimulation with acetylcholine and compare them with responses to cerulein in pancreatic tissue slices, with special emphasis on inter-cellular and inter-acinar heterogeneity and coupling. To this end, calcium imaging was performed employing confocal microscopy during stimulation with a wide range of acetylcholine concentrations and selected concentrations of cerulein. We show that various calcium oscillation parameters depend monotonically on the stimulus concentration and that the activity is rather well synchronized within acini, but not between acini. The acute pancreas tissue slice represents a viable and reliable experimental approach for the evaluation of both intra- and inter-cellular signaling characteristics of acinar cell calcium dynamics. It can be utilized to assess many cells simultaneously with a high spatiotemporal resolution, thus providing an efficient and high-yield platform for future studies of normal acinar cell biology, pathophysiology, and screening pharmacological substances.
Terjedelem/Fizikai jellemzők:Terjedelem: 26 p.-Azonosító: 0268644
ISSN:1932-6203