2025/11/15
paper · doi:10.17912/micropub.biology.001883
<p>Calcium signaling is an important regulator of stem cell maintenance and differentiation. Here we report the development of an image processing pipeline for <i>ex vivo</i> time-lapse microscopy data that enables the unbiased, automated detection of calcium signaling events in prohemocytes of the <i>Drosophila melanogaster </i>lymph gland. We also show that heterogeneity in gene expression driven by Tep4-Gal4, which is used to mark prohemocytes, accounts for most of the cell-to-cell variability in the signal, and that spontaneous calcium signaling events in the lymph gland can last from a few seconds to well over a minute.</p>