Schrezenmeir J, Hering B J, Gerö L, Wiegand-Dressler J, Solhdju M, Velten F, Kirchgessner J, Laue C, Beyer J, Bretzel R
III. Med. Klinik und Poliklinik, Innere Medizin und Endokrinologie, Johannes Gutenberg Universität Mainz, Germany.
Horm Metab Res. 1993 Apr;25(4):204-9. doi: 10.1055/s-2007-1002077.
The influence of alginate-embedding on the maintenance of functioning and morphological integrity in long-term culture of isolated porcine islets and islet cells was studied. Free-floating islets and islet cells served for control. Function was tested after the 1st, 2nd and 4th week. Basal and glucose-stimulated insulin secretion of embedded islets decreased slightly, but significantly after the first week (from 4.39 +/- 0.64 to 2.87 +/- 0.47 at normal and from 11.96 +/- 1.44 to 4.76 +/- 0.78 microU pro 24 h pro islet at elevated glucose concentration, p < 0.05 and < 0.01, resp.) and remained unchanged thereafter. Glucose-stimulation resulted in significant increases in insulin secretion at all three testings (p < 0.001, < 0.01 and < 0.01). Single cells in alginate matrix had even more stable insulin secretion throughout the whole cultivation with significant increases to glucose challenge (p < 0.01, < 0.01 and < 0.05). In contrast, insulin secretion of free-floating islet cells decreased from 5.70 +/- 1.19 to 2.04 +/- 0.64 and to 1.05 +/- 0.33 at basal conditions (p < 0.01 and < 0.05) and from 11.39 +/- 1.87 to 2.76 +/- 0.76 and to 2.15 +/- 0.71 microU pro 24 h pro islet under stimulation (p < 0.01 and not sign). In addition, the secretory response to glucose challenge was significant only at the first testing (p < 0.05). Non-embedded islets could be tested only at the first week since after this time they dissociated to single cells. Embedded islets and single cells showed intact morphology after four weeks with trypan blue (TPB) positivity of less than 5%.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了藻酸盐包埋对分离的猪胰岛和胰岛细胞长期培养中功能及形态完整性维持的影响。游离的胰岛和胰岛细胞作为对照。在第1、2和4周后测试功能。包埋胰岛的基础胰岛素分泌和葡萄糖刺激的胰岛素分泌在第一周后略有下降,但显著下降(正常情况下从4.39±0.64降至2.87±0.47,高葡萄糖浓度下从11.96±1.44降至4.76±0.78微单位/24小时/胰岛,分别为p<0.05和<0.01),此后保持不变。在所有三次测试中,葡萄糖刺激均导致胰岛素分泌显著增加(p<0.001、<0.01和<0.01)。藻酸盐基质中的单细胞在整个培养过程中胰岛素分泌更稳定,对葡萄糖刺激有显著增加(p<0.01、<0.01和<0.05)。相比之下,游离胰岛细胞在基础条件下的胰岛素分泌从5.70±1.19降至2.04±0.64,再降至1.05±0.33(p<0.01和<0.05),在刺激下从11.39±1.87降至2.76±0.76,再降至2.15±0.71微单位/24小时/胰岛(p<0.01和无显著性差异)。此外,对葡萄糖刺激的分泌反应仅在第一次测试时有显著性(p<0.05)。未包埋的胰岛仅在第一周可进行测试,因为此后它们会解离为单细胞。四周后,包埋的胰岛和单细胞经台盼蓝(TPB)检测显示形态完整,阳性率低于5%。(摘要截断于250字)