Parsa I, Marsh W H, Sutton A L, Butt K M
Am J Pathol. 1981 Mar;102(3):403-11.
Portions of adult human pancreas from 20 donors were organ-cultured in a chemically defined medium in the absence or presence of DMNA for up to 12 weeks. In the absence of DMNA, necrosis of some acini occurred during the first week, while some clusters of well-preserved acini were maintained for up to 3 weeks. Proliferation of the epithelial linings of main and smaller ducts and ductules was noted during the first 2 weeks of culture. Ductal epitheliums thereafter showed some degeneration but remained viable during the 12 weeks of culture. In contrast to controls, the DMNA-treated explants showed better preservation of both acinar and ductal cells. DMNA induced both ductal hyperplasia and atypia of the epithelial linings of main ducts, smaller ducts, and ductules within 6 weeks, and carcinoma by the tenth week of culture. At the end of the first week cells devoid of zymogen within the acinar complex proliferated and progressively replaced necrotic cells. During the ninth and tenth weeks, foci of atypical cells developed among these cells. Cells derived from 10-week-old DMNA-treated explants produced multiple nodules of carcinoma when injected subcutaneously into nude mice.
取自20位供体的成人胰腺组织在化学成分明确的培养基中进行器官培养,培养时间长达12周,培养过程中分别设置有无二甲基亚硝胺(DMNA)的条件。在无DMNA的情况下,培养第一周时一些腺泡出现坏死,而一些保存良好的腺泡簇可持续存在3周。在培养的前两周,可见主导管及较小导管和小胆管的上皮细胞增殖。此后,导管上皮出现一些退变,但在12周的培养期内仍保持存活。与对照组相比,经DMNA处理的外植体中腺泡细胞和导管细胞的保存情况更好。DMNA在6周内诱导主导管、较小导管和小胆管的上皮细胞出现导管增生和异型性,培养至第10周时诱导产生癌。在第一周结束时,腺泡复合体中无酶原的细胞增殖并逐渐取代坏死细胞。在第九周和第十周期间,这些细胞中出现了非典型细胞灶。将来自经DMNA处理10周的外植体的细胞皮下注射到裸鼠体内后,可产生多个癌结节。