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Lab-Grown Embryo Creates Human Blood Cells for Regenerative Medicine

by Rachel Kim – Technology Editor

Lab-Grown Human Embryo Model Yields Functional Blood Cells

Researchers at⁢ the University of Cambridge’s Gurdon Institute have successfully grown ‍embryo-like structures in the lab capable of producing human blood cells, a breakthrough with notable implications for regenerative medicine.⁤ The findings were published in Cell Reports on [Date not explicitly stated, but implied to be around publication date of the link: 2025].

The team, led by Dr. Jitesh Neupane ⁢and Prof. Azim Surani, utilized human stem cells -‍ which can be derived from any cell in ‌the ‍body – to create these models, replicating aspects of human​ development ⁣occurring ‍between the third and fourth weeks of pregnancy. Crucially, the models were designed without the tissues necessary to form a placenta or yolk sac, and lacked the potential ‍to develop⁢ into a ⁣foetus or brain, representing a “minimalistic system” according to​ Dr. Neupane.

Within two days, ‌the stem cells self-organized into the three primary germ layers – ectoderm, mesoderm, and endoderm – foundational to body plan development. By day eight, beating heart cells emerged. Though, it was on day 13‌ that a visually ‍striking development‍ occurred: the appearance of red patches indicating blood cell formation.

Further analysis confirmed the ​production of functional blood⁢ stem cells ‍within the model, capable of differentiating ‍into various blood cell types, including oxygen-carrying red blood cells and immune-system critical white blood cells. ‌Dr. Neupane described the moment the blood appeared as “exciting,” noting its visibility even⁣ to the naked eye.

This new method differs from existing laboratory techniques for⁤ generating human blood stem cells by⁣ mimicking natural developmental processes, relying on ⁤self-organizing structures rather than requiring added proteins. Researchers believe this advance⁢ could ultimately lead to bone marrow transplant therapies⁣ utilizing a patient’s own cells, eliminating compatibility issues.

Prof. Surani emphasized the significance ‌of this work as a “significant step towards future regenerative therapies,” offering potential for screening drugs, studying early blood ​and ‍immune development, and modeling blood disorders like leukemia.

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