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Cryopreservation of human fetal organs
Authors:Peter Groscurth   Miriam Erni   Marina Balzer   Hans-Jakob Peter  Gisela Haselbacher
Affiliation:(1) Division of Cell Biology, Department of Anatomy, University of Zürich, Zürich, Switzerland;(2) Laboratory of Endocrinology, Clinic of Medicine, University Hospital Bern, Bern, Germany;(3) Department of Biochemistry, University of Zürich, Switzerland
Abstract:
Summary The effects of low temperature preservation on morphology, viability and differentiation capacity of different human fetal organs were studied using transmission (TEM) and scanning (SEM) electron microscopy, in vitro cultivation as well as xenogeneic transplantation. For this purpose fragments of lung, kidney, small intestine, thyroid, brain, liver and spleen from 10 human fetuses (aged 9 to 14 weeks of gestation) were frozen by a three step cooling procedure. After 3 to 12 months the specimens were thawed rapidly and processed for TEM and/or in vitro cultivation and/or transplantation into nude mice. TEM studies on frozen lung, kidney and intestine revealed generally a well preserved ultrastructure whereas liver and spleen fragments appeared highly necrotic. From three fetuses, frozen intestine and lung specimens were used for the establishment of monolayer cultures. Following trypsinization, both epithelial and mesenchymal cells formed a continous layer on the bottom of plastic bottles. During further subpassages the number of epithelial cells decreased resulting in the formation of pure fibroblast cultures. Frozen brain tissue from one fetus was also successfully cultivated forming cell clusters and fiber bundles of variable size at the surface of glass cover slips. Following subcutaneous implantation into nude mice, the vast majority of fragments from lung, kidney, intestine and thyroid was found to growth in the recipients. The growth of xenografts was accompanied by persistence (kidney, intestine) or even increase (lung, thyroid) in cellular differentiation studied by TEM or autoradiography. Transplanted liver and spleen fragments, however, regularly regressed forming solid scars in the subcutaneous tissue of nude mice.In summary, the three-step cooling procedure is an effective method for storage of different human fetal organs preserving morphology, viability and differentiation capacity of the tissues. Thawed specimens may be used for several experiments including in vivo and in vitro studies.In memoriam Prof. Dr. med. G. Töndury, dagger 15.3.1985
Keywords:Cryopreservation  Human fetuses  Nude mouse
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