Chen Lih-Ju, Su Yi-An, Lin Ting-Hui, Liao Wan-Ting, Wu Chun-Chi, Lin Chen-Chu, Chen Chang-Han, Hsu Tsai-Ching, Yang Ya-Wen, Lee Yi-Ju
Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung 402, Taiwan.
Division of Neonatology, Changhua Christian Children's Hospital, Changhua 500, Taiwan.
Biomedicines. 2025 Jun 12;13(6):1455. doi: 10.3390/biomedicines13061455.
: The principal function of mammary glands is to produce milk to nourish the newborn. Optimal lactation is controlled by various hormones, growth factors, and cytokines. : Using 3D cultures of primary mouse mammary epithelial cells, we explored the effects of T helper (Th)1 cytokines, interferon (IFN)-γ, and tumor necrosis factor (TNF)-α on the structure and function of mammary cells as well as the underlying mechanism. : Three-dimensional cultures of mammary cells were treated with IFN-γ/TNF-α, and milk protein expression and acinar structures were analyzed by immunoblotting and immunofluorescence microscopy. : Our results revealed that combined treatment with IFN-γ and TNF-α inhibits prolactin-induced STAT5 tyrosine phosphorylation and β-casein expression. These cytokines also disrupted the structure of mammary acini, resulting in smaller or no lumens, disordered cell arrangements, and multilayered cells in certain regions. Additionally, some cells became elongated rather than maintaining their usual cube-like shape. Since cell proliferation and death can modulate the structural organization of acini, we examined the influences of IFN-γ and TNF-α on these events. Combined cytokine treatment moderately increased cell proliferation and cell death. Notably, stimulation with IFN-γ and TNF-α induced the expression of inducible nitric oxide synthase (iNOS), and the inhibition of iNOS partially restored acinar morphology and β-casein expression, revealing a novel mechanism for cytokine-induced acinar disruption. : When a Th1 cytokine milieu is dominant, such as during inflammation and infection, IFN-γ and TNF-α might cause mammary gland ductal occlusion and lactation insufficiency.
乳腺的主要功能是分泌乳汁以滋养新生儿。最佳泌乳受多种激素、生长因子和细胞因子调控。
我们利用原代小鼠乳腺上皮细胞的三维培养,探究辅助性T细胞(Th)1细胞因子、干扰素(IFN)-γ和肿瘤坏死因子(TNF)-α对乳腺细胞结构和功能的影响及其潜在机制。
用IFN-γ/TNF-α处理乳腺细胞的三维培养物,通过免疫印迹和免疫荧光显微镜分析乳蛋白表达和腺泡结构。
我们的结果显示,IFN-γ和TNF-α联合处理可抑制催乳素诱导的信号转导和转录激活因子5(STAT5)酪氨酸磷酸化及β-酪蛋白表达。这些细胞因子还破坏了乳腺腺泡的结构,导致管腔变小或消失、细胞排列紊乱以及某些区域出现细胞多层化。此外,一些细胞变得细长,而非保持其通常的立方体形。由于细胞增殖和死亡可调节腺泡的结构组织,我们研究了IFN-γ和TNF-α对这些过程的影响。细胞因子联合处理适度增加了细胞增殖和细胞死亡。值得注意的是,IFN-γ和TNF-α刺激诱导了诱导型一氧化氮合酶(iNOS)的表达,抑制iNOS可部分恢复腺泡形态和β-酪蛋白表达,揭示了细胞因子诱导腺泡破坏的新机制。
当Th1细胞因子环境占主导时,如在炎症和感染期间,IFN-γ和TNF-α可能导致乳腺导管闭塞和泌乳不足。