Arkansas Children's Nutrition Center, Little Rock, AR, USA.
Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
J Nutr. 2020 Apr 1;150(4):730-738. doi: 10.1093/jn/nxz273.
Soy infant formula contains isoflavones, which are able to bind to and activate estrogen receptor (ER) pathways. The mammary gland is sensitive to estrogens, raising concern that the use of soy formulas may promote premature development.
We aimed to determine if soy formula feeding increases mammary gland proliferation and differentiation in comparison to other infant postnatal diets.
White-Dutch Landrace piglets aged 2 d received either sow milk (Sow), or were provided milk formula (Milk), soy formula (Soy), milk formula supplemented with 17-beta-estradiol (2 mg/(kg·d); M + E2), or milk formula supplemented with genistein (84 mg/L of diet; M + G) until day 21. Mammary gland proliferation and differentiation was assessed by histology, and real-time RT-PCR confirmation of differentially expressed genes identified by microarray analysis.
Mammary terminal end bud numbers were 19-31% greater in the Milk, Soy, and M + G groups relative to the Sow and M + E2, P <0.05. Microarray analysis identified differentially expressed genes between each formula-fed group relative to the Sow (±1.7-fold, P <0.05). Real-time RT-PCR confirmed 2- to 4-fold increases in mRNA transcripts of genes involved in cell proliferation, insulin-like growth factor 1 (IGF1), fibroblast growth factor 10 (FGF10), and fibroblast growth factor 18 (FGF18), in all groups relative to the Sow, P <0.05. In contrast, genes involved in cell differentiation and ductal morphogenesis, angiotensin II receptor type 2 (AGTR2), microtubule associated protein 1b (MAP1B), and kinesin family member 26b (KIF26B), were significantly upregulated by 2-, 4-, and 13-fold, respectively, in the M + E2 group. Additionally, mRNA expression of ER-specific gene targets, progesterone receptor (PGR), was increased by 12-fold, and amphiregulin (AREG) and Ras-like estrogen regulated growth inhibitor (RERG) expression by 1.5-fold in the M + E2 group, P <0.05. In the soy and M + G groups, mRNA expressions of fatty acid synthesis genes were increased 2- to 4-fold.
Our data indicate soy formula feeding does not promote ER-signaling in the piglet mammary gland. Infant formula feeding (milk- or soy-based) may initiate proliferative pathways independently of estrogenic signaling.
大豆婴儿配方奶粉含有异黄酮,能够与雌激素受体(ER)途径结合并激活该途径。乳腺对雌激素敏感,这引起了人们的关注,即使用大豆配方奶粉可能会促进过早发育。
我们旨在确定与其他婴儿产后饮食相比,大豆配方奶粉喂养是否会增加乳腺增殖和分化。
2 日龄的白荷兰兰德瑞斯仔猪接受母猪奶(Sow)或提供牛奶配方奶粉(Milk)、大豆配方奶粉(Soy)、添加 17-β-雌二醇(2 mg/(kg·d);M+E2)的牛奶配方奶粉或添加染料木黄酮(84 mg/L 饮食;M+G)的牛奶配方奶粉,直至 21 天。通过组织学评估乳腺终末芽的增殖和分化,并通过实时 RT-PCR 确认微阵列分析确定的差异表达基因。
与 Sow 和 M+E2 相比,Milk、Soy 和 M+G 组的乳腺终末芽数量增加了 19-31%,P<0.05。微阵列分析确定了每个配方喂养组与 Sow 之间差异表达的基因(±1.7 倍,P<0.05)。实时 RT-PCR 证实,与 Sow 相比,所有组的细胞增殖、胰岛素样生长因子 1(IGF1)、成纤维细胞生长因子 10(FGF10)和成纤维细胞生长因子 18(FGF18)相关基因的 mRNA 转录均增加了 2-4 倍,P<0.05。相反,参与细胞分化和导管形态发生的基因,血管紧张素 II 受体 2(AGTR2)、微管相关蛋白 1b(MAP1B)和驱动蛋白家族成员 26b(KIF26B),在 M+E2 组中分别上调了 2、4 和 13 倍,P<0.05。此外,M+E2 组孕激素受体(PGR)的 ER 特异性基因靶标、孕激素受体(PGR)和 Ras 样雌激素调节生长抑制剂(RERG)的表达增加了 12 倍和 1.5 倍,P<0.05。在大豆和 M+G 组中,脂肪酸合成基因的 mRNA 表达增加了 2-4 倍。
我们的数据表明,大豆配方奶粉喂养不会促进猪乳腺中的 ER 信号。婴儿配方奶粉喂养(牛奶或大豆基)可能独立于雌激素信号启动增殖途径。