Publications by authors named "Astar Lazmi Hailu"

Article Synopsis
  • Stem cell therapies for cartilage disease are hindered by a lack of understanding of cartilage formation and maintenance.
  • Human bone marrow stromal cells (hBMSCs) can create stable cartilage when using hyaluronic acid-coated microbeads, but the exact mechanisms are not fully understood.
  • Although hBMSCs failed to repair cartilage in rodents, cells derived from chondrospheroids showed promising results by forming lasting non-hypertrophic cartilage.
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Skin exposure to high-dose irradiation, as commonly practiced in radiotherapy, affects the different skin layers, causing dry and wet desquamation, hyperkeratosis fibrosis, hard to heal wounds and alopecia and damaged hair follicles. Fetal tissue mesenchymal stromal cells (f-hPSC) were isolated from excised human fetal placental tissue, based on their direct migration from the tissue samples to the tissue dish. The current study follows earlier reports on for the mitigation of acute radiation syndrome following whole body high-dose exposure with remotely injected f-hPSC.

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Purpose: Selected placental mesenchymal stromal cells isolated from the fetal mesenchymal placental tissues (f-hPSCs) were tested as cell therapy of lethal acute radiation syndrome (ARS) with bone marrow regeneration and induced extramedullary hematopoiesis.

Methods And Materials: f-hPSCs were isolated from the chorionic plate of human placentae and further expanded in regular culture conditions. 2 × 10 f-hPSCs were injected on days 1 and 4 to 8-Gy total body irradiated (TBI) C3H mice, both intramuscularly and subcutaneously.

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The injection of placental stromal cells isolated from fetal human tissues (f-hPSC) was reported to indirectly induce tissue regeneration in different animal models. A procedure of f-hPSC isolation from fragments of both selected fresh or cryopreserved bulk placental neonate tissues is proposed, based on their high migratory potential,. The fragments of the desired fetal placental tissues are adhered to a culture dish by traces of diluted fibrin and covered with culture medium.

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