Department of Animal Science, Michigan State University, East Lansing, MI 48824, USA.
J Anim Sci. 2012 Jan;90(1):221-30. doi: 10.2527/jas.2011-4179. Epub 2011 Aug 5.
Prolactin, glucocorticoids, and insulin are commonly used to induce milk protein synthesis in bovine mammary cell cultures. In addition, administration of GH increases milk yield in dairy cows, likely via the mammalian target of rapamycin (mTOR) pathway and IGF-I synthesis. As such, the hypothesis of this study was that mRNA abundance of hormone receptors, mammalian target of mTOR pathway-related kinases, IGF-I, and milk protein-encoding genes increases in the porcine mammary gland in response to greater lactation demand. Selected genes included those encoding for receptors of GH (GHR), insulin (INSR), glucocorticoid (NR3C1), prolactin (PRLR), IGF-I (IGF-I), mTOR (FRAP1), and p70S6 kinases (RPS6KB1), and the milk proteins α-lactalbumin (LALBA) and β-casein (CSN2). Mammary tissue was biopsied from 4 sows on d 110 of gestation (prepartum), d 5 and 17 of lactation, and d 5 after weaning (postweaning), and gene expression was quantified by reverse-transcription quantitative PCR. Compared with prepartum, d 5 of lactation increased (P < 0.001) NR3C1, tended to increase (P = 0.06) GHR, and decreased (P < 0.001) PRLR mRNA abundance. Compared with d 5 of lactation, d 17 of lactation increased PRLR (P < 0.001) and decreased GHR (P < 0.01). Expression of INR and FRAP1 did not differ when comparing either prepartum or d 17 of lactation with d 5 of lactation. Compared with d 17 of lactation, postweaning decreased (P < 0.001) PRLR, did not affect INSR, and increased both IGF-I and GHR (P < 0.05) mRNA abundance. From prepartum to d 17 of lactation, NR3C1 mRNA abundance was positively correlated with CSN2 (r = 0.85; P < 0.001) and LALBA mRNA abundance (r = 0.79; P = 0.002), whereas mRNA abundance of GHR tended to be positively correlated with that of IGF-I (r = 0.46; P = 0.06). In conclusion, expression of the genes NR3C1, PRLR, GHR, and IGF-I changed in the porcine mammary gland during the prepartum to postweaning periods, but only NR3C1 mRNA abundance was positively correlated with expression of CSN2 and LALBA.
催乳素、糖皮质激素和胰岛素通常用于诱导牛乳腺细胞培养物中的乳蛋白合成。此外,生长激素(GH)的给药增加了奶牛的产奶量,这可能是通过哺乳动物雷帕霉素靶蛋白(mTOR)途径和 IGF-I 合成实现的。因此,本研究的假设是,随着泌乳需求的增加,猪乳腺中激素受体、mTOR 途径相关激酶、IGF-I 和乳蛋白编码基因的 mRNA 丰度增加。选择的基因包括编码 GH(GHR)、胰岛素(INSR)、糖皮质激素(NR3C1)、催乳素(PRLR)、IGF-I(IGF-I)、mTOR(FRAP1)和 p70S6 激酶(RPS6KB1)的受体,以及乳蛋白α-乳白蛋白(LALBA)和β-酪蛋白(CSN2)。在妊娠第 110 天(产前)、第 5 天和第 17 天泌乳以及断奶后第 5 天(断奶后)从 4 头母猪中采集乳腺组织,并通过逆转录定量 PCR 定量基因表达。与产前相比,泌乳第 5 天 NR3C1 mRNA 丰度增加(P < 0.001),GHR 趋于增加(P = 0.06),PRLR mRNA 丰度降低(P < 0.001)。与泌乳第 5 天相比,泌乳第 17 天 PRLR 增加(P < 0.001),GHR 减少(P < 0.01)。与泌乳第 17 天相比,断奶后 PRLR 减少(P < 0.001),INSR 不受影响,IGF-I 和 GHR mRNA 丰度增加(P < 0.05)。从产前到泌乳第 17 天,NR3C1 mRNA 丰度与 CSN2(r = 0.85;P < 0.001)和 LALBA mRNA 丰度呈正相关(r = 0.79;P = 0.002),而 GHR mRNA 丰度趋于与 IGF-I 的正相关(r = 0.46;P = 0.06)。总之,NR3C1、PRLR、GHR 和 IGF-I 基因的表达在猪乳腺从产前到断奶后期间发生变化,但只有 NR3C1 mRNA 丰度与 CSN2 和 LALBA 的表达呈正相关。