Keys J E, Fekry A E, Wood D L, Capuco A V
Milk Secretion and Mastitis Laboratory, U.S. Department of Agriculture, Beltsville, MD 20705.
Biochem Cell Biol. 1992 May;70(5):343-6. doi: 10.1139/o92-053.
Explants of bovine mammary, liver, and adipose tissues were cocultured in the same well for 24, 48, 72 or 96 h and their ability to synthesize lipids was measured by the incorporation of [14C]acetate into triglycerides, free fatty acids, and phospholipids. The model was developed to study the effect of bovine somatotropin on lipid synthesis in mammary tissue, because somatotropin will not affect mammary tissue unless liver tissue is present. Somatotropin reduced incorporation by mammary tissue relative to the control. However, the rate of incorporation remained constant through 96 h with somatotropin, but steadily decreased in control mammary tissue. Phospholipid release into the media increased dramatically from 2% of that synthesized during the first 24 h to 218% of that synthesized from 72 to 96 h. The high release of phospholipids after 24 h suggests that cellular breakdown was occurring. A 24-h incubation is recommended to study lipid synthesis with this system.
将牛乳腺、肝脏和脂肪组织的外植体在同一孔中共同培养24、48、72或96小时,并通过将[14C]乙酸掺入甘油三酯、游离脂肪酸和磷脂中来测量它们合成脂质的能力。开发该模型是为了研究牛生长激素对乳腺组织脂质合成的影响,因为生长激素除非有肝脏组织存在,否则不会影响乳腺组织。相对于对照组,生长激素降低了乳腺组织的掺入量。然而,在添加生长激素的情况下,掺入率在96小时内保持恒定,但在对照乳腺组织中则稳步下降。释放到培养基中的磷脂从最初24小时合成量的2%急剧增加到72至96小时合成量的218%。24小时后磷脂的高释放表明细胞正在分解。建议使用该系统进行24小时孵育以研究脂质合成。