作者: Giovanni Luca , Mario Calvitti , Giuseppe Basta , Tiziano Baroni , Luca M. Neri
DOI: 10.1136/JIM-51-02-09
关键词: Insulin 、 Venom 、 Islet 、 Fluorescein 、 Biology 、 In vitro 、 Endocrinology 、 Monoclonal antibody 、 Incubation 、 Internal medicine 、 Immunolabeling
摘要: Background One of the major pitfalls associated with use isolated adult islets Langerhans9 cells is their minimal mitotic capacity. Consequently, maintenance a steady viable islet cell mass very difficult. To explore how to enhance beta-cell mitoge-nesis, we have examined effects venom fractions extracted from Brazilian scorpion on morphologic and functional patterns. The was previously known induce nesidioblas-tosis-like chronic hypoglycemia pancreatitis in animal models. Methods Venom purified Tityus bahiensis were incubated batches rat islets, while examination, glucose-stimulated insulin release, content, messenger ribonucleic acid (mRNA) carried out early during incubation. On fixation double fluorescence immunolabeling (rhodamine for anti-insulin monoclonal antibodies; fluorescein anti-5-bromodeoxyuridine), preparations imaged by confocal laser microscopy (CLM) morphome- trie quantification mitoses. Insulin recovery mRNA also assessed at 21 days culture. Results Under CLM rate significantly rose 1 12.8% venom-exposed islets. At day 7, release content lower than control However, culture, response static incubation glucose higher controls (p Conclusions Incubation induced rapid significant increase proliferation not short-term secretion. latter fully resumed overcame later possibly after completion expansion process.