Rosenberg L, Vinik A I
Department of Surgery, Montreal General Hospital, McGill University, Quebec, Canada.
Pancreas. 1993 Mar;8(2):255-60. doi: 10.1097/00006676-199303000-00018.
Partial obstruction of the hamster pancreas in the cellophane wrap model leads to the induction of duct and ductular proliferation followed by endocrine cell differentiation. This effect appears to be mediated by the local action of a growth factor. The purpose of the present study was to determine if cytosolic extract prepared from the wrapped pancreas had trophic activity on purified hamster pancreatic ductal epithelium in tissue culture. Cultures of purified pancreatic ducts were prepared by digestion of the hamster pancreas using a solution of collagenase type XI and chymotrypsin infused directly into the pancreatic duct. The ducts were separated and purified by a series of steel mesh filtrations. Ducts were embedded in 1.5% Seaplaque agarose and fed a liquid medium containing serum-free Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12 Ham (DME/F-12), 12.5% cytosol extract+DME/F-12, or 25% cytosol extract+DME/F-12. The trophic effect of the extract on the tissue in culture was evaluated by the incorporation of tritiated thymidine ([3H]TdR) into DNA. Duct fragments cultured in medium supplemented with 12.5% cytosol showed no difference in their [3H]TdR uptake compared with control ducts (908 +/- 147 vs. 913 +/- 151 dpm/micrograms DNA). The incorporation of [3H]TdR by ducts maintained in medium supplemented with 25% cytosol extract was increased 78% over serum-free controls (1,632 +/- 386 vs. 913 +/- 147 dpm/micrograms DNA; p < 0.025). We conclude that a cytosol extract prepared from the partially obstructed cellophane-wrapped pancreas contains a factor(s) trophic for pancreatic ductal cells.
在玻璃纸包裹模型中,仓鼠胰腺的部分梗阻会导致导管和小导管增生,随后出现内分泌细胞分化。这种效应似乎是由一种生长因子的局部作用介导的。本研究的目的是确定从包裹的胰腺制备的胞质提取物在组织培养中对纯化的仓鼠胰腺导管上皮是否具有营养活性。通过使用直接注入胰腺导管的XI型胶原酶和胰凝乳蛋白酶溶液消化仓鼠胰腺来制备纯化的胰腺导管培养物。通过一系列钢网过滤分离并纯化导管。将导管包埋在1.5%的Seaplaque琼脂糖中,并给予含有无血清杜氏改良 Eagle 培养基/营养混合物F-12仓鼠培养基(DME/F-12)、12.5%胞质提取物+DME/F-12或25%胞质提取物+DME/F-12的液体培养基。通过将氚标记的胸腺嘧啶核苷([3H]TdR)掺入DNA来评估提取物对培养组织的营养作用。与对照导管相比,在补充有12.5%胞质的培养基中培养的导管片段在[3H]TdR摄取方面没有差异(908±147对913±151 dpm/μg DNA)。在补充有25%胞质提取物的培养基中培养的导管,其[3H]TdR掺入量比无血清对照增加了78%(1632±386对913±147 dpm/μg DNA;p<0.025)。我们得出结论,从部分梗阻的玻璃纸包裹胰腺制备的胞质提取物含有对胰腺导管细胞具有营养作用的一种或多种因子。