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Habib, S. J.

Publications and source records attributed to Habib, S. J..

4 recordsLinked to original sources

Benchmarking Machine Learning and Automated Image Analysis for Organelle Quantification

Quantitative organelle analysis is highly sensitive to image-processing choices, limiting reproducibility across microscopy studies. Here, we systematically compare automated, interactive machine learning, and deep learning-based pipelines for lipid droplet and mitochondrial quantification in live human osteosarcoma cells imaged by fluorescence microscopy and label-free holotomography. Using standardized downstream feature extraction, we evaluated script-based workflows (Fiji, Python), a modular platform (CellProfiler), interactive machine learning (ilastik), and pretrained deep learning models. Lipid droplet segmentation was qualitatively consistent across approaches; however, droplet counts, and size distributions varied substantially between pipelines and imaging modalities, with ilastik reducing background-driven detections and improving cross-modality agreement. In contrast, mitochondrial quantification proved highly sensitive to segmentation and skeletonization choices, particularly in holotomography where global intensity-threshold-based methods failed to capture network structure. Based on these cross-pipeline comparisons, we demonstrate how organelle- and modality-specific benchmarking can guide pipeline selection, illustrated by the analysis of metabolic perturbations affecting lipid droplets and mitochondria. Together, these results highlight modality- and morphology-dependent limitations in common analysis pipelines and provide practical guidance for selecting robust, reproducible strategies for quantitative organelle imaging.

cell biology↗

Wnt-presenting materials sustain H3K14-acetylation in human skeletal stem cells for tissue engineering and bone repair

Engineering functional tissues for transplantation requires insight into epigenetic mechanisms that regulate stem cell fate. We have developed the Wnt-induced osteogenic tissue model (WIOTM), a platform that recapitulates human osteogenesis, and identified acetylation of histone H3 at lysine 14 (H3K14ac) as a critical epigenetic regulator in human skeletal stem cells (hSSCs). In WIOTM, localized Wnt signals drive asymmetric cell division (ACD), yielding a proximal hSSC with high H3K14ac and a distal daughter with reduced H3K14ac that migrates into the 3D collagen matrix and initiates osteogenic differentiation. Disrupting H3K14ac in hSSCs abrogates ACD and WIOTM formation. To test whether hSSCs maintain H3K14ac in vivo, we formed the WIOTM on Wnt-functionalized polymer bandages and transplanted them into calvarial defects. The WIOTM contributed to bone repair, and human cells adjacent to the bandages retained high H3K14ac despite the injury environment. These findings establish WIOTM as both a mechanistic and translational platform for regenerative medicine.

cell biology↗

Geometrical Designs in Volumetric Bioprinting to Study Cellular Behaviors in Engineered Constructs

This study investigates the influence of geometrical variations in volumetrically printed (Vol3DP) structures on the attachment, survival, and organization of cancer cells (143b) and human umbilical vein endothelial cells (HUVECs). We adapted a gelatin methacryloyl (GelMA)-poly(ethylene glycol) diacrylate (Gel-PEG) resin for volumetric bioprinting. Compared to GelMA, Gel-PEG improved printing fidelity and resolution, superior mechanical properties, and reduced swelling. We fabricated disc-like constructs and channel geometries, including straight channels and angular designs of 60{degrees}, 90{degrees}, and 110{degrees} and cultured human umbilical vein endothelial cells (HUVECs) and 143b human osteosarcoma cells, a highly metastatic cell line, for up to 14 days. Using label-free holographic microscopy, we visualized cellular protrusions, important for adhesion and mechanosensing, in real-time and without staining, an advantage for long-term, live-cell analysis in 3D constructs. HUVECs adhered well, expressed CD31, and showed preferential spreading in channels with specific geometrical angles, indicating geometry-sensitive behavior. This is physiologically relevant, as it reflects the native mechanosensitive and alignment behavior of endothelial cells during vascular formation. In contrast, osteosarcoma cells spread uniformly throughout the constructs, formed dense, geometry-independent agglomerates, and exhibited enhanced growth and spreading within the Gel-PEG matrix compared to GelMA. This behavior is consistent with the aggressive and geometry-insensitive nature of metastatic tumor cells. These findings highlight Gel-PEGs utility for generating stable, biomimetic 3D environments and demonstrate the application of holographic microscopy for assessing cell- material interactions within volumetrically bioprinted constructs, underscoring the potential of this approach for developing vascularized models and studying mechanobiological responses in engineered tissues. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=193 SRC="FIGDIR/small/664683v1_ufig1.gif" ALT="Figure 1"> View larger version (64K): org.highwire.dtl.DTLVardef@9e3820org.highwire.dtl.DTLVardef@176eb5aorg.highwire.dtl.DTLVardef@558764org.highwire.dtl.DTLVardef@12bc5cb_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗

Rejuvenating aged osteoprogenitors for bone repair

Aging is marked by a decline in tissue regeneration, posing significant challenges to an increasingly older population. Here, we investigate age-related impairments in calvarial bone healing and introduce a novel two-part rejuvenation strategy to restore youthful repair. We demonstrate that aging negatively impacts the calvarial bone structure and its osteogenic tissues, diminishing osteoprogenitor number and function and severely impairing bone formation. Notably, increasing osteogenic cell numbers locally fails to rescue repair in aged mice, identifying the presence of intrinsic cellular deficits. Our strategy combines Wnt-mediated osteoprogenitor expansion with intermittent fasting, which leads to a striking restoration of youthful levels of bone healing. We find that intermittent fasting improves osteoprogenitor function, benefits that can be recapitulated by modulating NAD+ dependent pathways or the gut microbiota, underscoring the multifaceted nature of this intervention. Mechanistically, we identify mitochondrial dysfunction as a key component in age-related decline in osteoprogenitor function and show that both cyclical nutrient deprivation and Nicotinamide mononucleotide rejuvenate mitochondrial health, enhancing osteogenesis. These findings offer a promising therapeutic avenue for restoring youthful bone repair in aged individuals, with potential implications for rejuvenating other tissues.

cell biology↗