Gat Rauner, Nicole C Traugh, Colin J Trepicchio, Meadow E Parrish, Kenan Mushayandebvu, Charlotte Kuperwasser
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引用次数: 0
Abstract
Current breast organoid models, primarily based on self-assembly, face limitations in accurately mimicking the complex stages of tissue development, notably in replicating detailed tissue architectures and cellular diversity. Here, we demonstrate that a solitary human breast stem cell can, within a controlled hydrogel extracellular matrix environment, autonomously generate niche signals that drive directed organogenesis, producing organoids with mesenchymal and parenchymal components. This system surpasses traditional models by forming complex, heterogeneous ductal-lobular structures akin to those in native human breast tissue with the emergence of mesenchyme-like stroma. Using long-term, high-resolution live imaging, we quantitatively analyze the dynamic tissue development and morphogenesis, capturing cellular behaviors crucial for understanding both development and disease. The inclusion of patient-derived cells from diverse biological backgrounds, including pre- and post-menopausal donors, significantly enhances the applicability of the model. Our findings underscore that this controlled organogenesis approach represents a major leap over existing methods, offering a robust platform for probing the intricacies of human breast tissue development and its responses to environmental cues.
期刊介绍:
Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community.
Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication.
To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.