Biology subjects

Wells, C. J.

Publications and source records attributed to Wells, C. J..

3 recordsLinked to original sources

bioRxiv2026

Altered stem cell properties of human hematopoietic stem and progenitor cells based on bone region location

The bone marrow microenvironment forms a highly specialized niche that houses hematopoietic stem and progenitor cells (HSPCs). Within bone, two anatomically distinct regions, the medullary cavity and the trabecular compartment, differ in their cellular and physical composition, with the potential to differentially regulate influence on resident HSPCs. We hypothesized that HSPCs enriched from the medullary cavity (BM) and trabeculae (TB) represent functionally distinct populations. Contrary to this, functional assessment of HSPCs revealed comparable cellular outputs between BM- and TB-derived HSPCs. To investigate whether microenvironmental signaling contributes to functional regulation, we examined the effects of extracellular vesicles (EVs) isolated from medullary BM and TB. Notably, TB-derived EVs inhibited cell cycle progression, directing HSPCs toward a quiescent state. Together, these findings demonstrate that while isolated BM- and TB-derived HSPCs exhibit similar cell-intrinsic properties, EVs enriched from the TB specifically promote HSPC quiescence, supporting a protective regulatory role for the trabecular microenvironment.

cell biology↗

bioRxiv2025

Fast, flexible, learning-free organoid quantification and tracking with OrganoSeg2

Organoids are routinely imaged by brightfield microscopy at low magnification, but these images are challenging to analyze quantitatively at scale. Given differences in organoid-culture format and image acquisition among research groups, there is a general need for versatile segmentation algorithms that refine for specific applications. Here, we introduce OrganoSeg2, an overhauled software that substantively advances the multi-window adaptive thresholding of its predecessor. OrganoSeg2 gives users access to additional segmentation parameters that were latent in OrganoSeg, and common operations are accelerated [~]10-fold. Using data from six organoid types, we find that the generalized segmentation accuracy of OrganoSeg2 surpasses multiple alternatives, including segmenters based on deep learning. OrganoSeg2 adds longitudinal single-organoid tracking and multicolor fluorescence quantification, which we use to examine growth trajectories and radiotherapy responses in luminal breast cancer organoids. OrganoSeg2 is shared freely as installation packages for current users and source code for future developers (https://github.com/JanesLab/OrganoSeg2). MOTIVATIONOrganoids are routinely documented with low-magnification brightfield and fluorescence images that are challenging to quantify accurately in large numbers. OrganoSeg2 is a streamlined, highly customizable segmenter that surpasses its prior version and AI-themed competitors in various organoid contexts. New longitudinal tracking and fluorescence capabilities of OrganoSeg2 are demonstrated with experiments investigating the cell-death responses of luminal breast cancer organoids to radiotherapy.

bioengineering↗

bioRxiv2025

Enriching for Extracellular Vesicles from Human Bone

Extracellular vesicles (EVs) are nano-sized membrane-bound structures thought to be secreted by all cells and increasingly recognized as key mediators of intercellular communication. Established EV isolation protocols for bodily fluids-primarily focus on blood with limited insights into methods optimized for EVs from other hematopoietic regions. In this study, we present a novel protocol for the isolation and enrichment of EVs from human trabecular bone and bone marrow. This method employs a two-step purification strategy, combining iodixanol density cushion (IDC) ultracentrifugation with size exclusion chromatography (SEC), and enables EV recovery from fresh tissue hours after collection. Importantly, this approach facilitates the enrichment of bone-derived EVs without the need for enzymatic digestion or long-term culture, preserving native EV populations. This protocol offers a valuable tool for researchers investigating EVs derived from the diverse cellular constituents of the bone microenvironment.

cell biology↗