细胞转录组学图谱提供了对猪乳腺脂肪细胞在整个发育过程中的见解。

IF 6.3 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Journal of Animal Science and Biotechnology Pub Date : 2023-10-08 DOI:10.1186/s40104-023-00926-0
Yongliang Fan, Long Jin, Zhiping He, Tiantian Wei, Tingting Luo, Jiaman Zhang, Can Liu, Changjiu Dai, Chao A, Yan Liang, Xuan Tao, Xuebin Lv, Yiren Gu, Mingzhou Li
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引用次数: 0

摘要

背景:研究乳腺的组成和发育机制对新生儿的健康成长至关重要。乳腺本质上是异质性的,其生理功能依赖于多种细胞类型的基因表达。大多数研究都集中在上皮细胞上,忽略了邻近脂肪细胞的作用。结果:在这里,我们构建了迄今为止最大的猪乳腺细胞转录组数据集。该数据集从五个发育阶段(妊娠90天,G90;哺乳后0天,L0;哺乳后20天,L20;自然退化后2天,PI2;自然退化前7天,PI7)的生理性乳腺中捕获了126829个高质量细胞核。鉴定出7种细胞类型,包括上皮细胞、脂肪细胞、内皮细胞、成纤维细胞、免疫细胞、肌上皮细胞和前体细胞。我们的数据表明,乳腺在不同的发育阶段具有不同的表型和转录特征。在妊娠晚期(G90),脂肪细胞的分化和增殖受到抑制。同时,部分上皮细胞完全分化。伪时间分析表明,上皮细胞经历三个阶段来达到泌乳,包括细胞分化、激素感应和代谢激活。在哺乳期(L0和L20),脂肪细胞面积占乳腺的0.5%以下。为了维持自身的生存,脂肪细胞表现出低分化状态和增殖能力。上皮细胞在激素刺激下开始泌乳。在完成泌乳任务后,它们在高强度泌乳下发生生理性死亡。有趣的是,生理性死亡细胞似乎通过CCL21-ACKR4途径被免疫细胞主动清除。这一生物学过程可能是维持乳腺稳态的重要机制。在自然退化过程中(PI2和PI7),上皮细胞群去分化为间充质干细胞,以在下一个哺乳周期保持乳腺的泌乳潜力。结论:从孕晚期到自然退化,揭示了脂肪细胞和上皮细胞去分化、增殖和再分化的分子机制。该细胞转录组学图谱为未来不同阶段乳腺发育和重塑的研究提供了重要参考。
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A cell transcriptomic profile provides insights into adipocytes of porcine mammary gland across development.

Background: Studying the composition and developmental mechanisms in mammary gland is crucial for healthy growth of newborns. The mammary gland is inherently heterogeneous, and its physiological function dependents on the gene expression of multiple cell types. Most studies focused on epithelial cells, disregarding the role of neighboring adipocytes.

Results: Here, we constructed the largest transcriptomic dataset of porcine mammary gland cells thus far. The dataset captured 126,829 high-quality nuclei from physiological mammary glands across five developmental stages (d 90 of gestation, G90; d 0 after lactation, L0; d 20 after lactation, L20; 2 d post natural involution, PI2; 7 d post natural involution, PI7). Seven cell types were identified, including epithelial cells, adipocytes, endothelial cells, fibroblasts cells, immune cells, myoepithelial cells and precursor cells. Our data indicate that mammary glands at different developmental stages have distinct phenotypic and transcriptional signatures. During late gestation (G90), the differentiation and proliferation of adipocytes were inhibited. Meanwhile, partly epithelial cells were completely differentiated. Pseudo-time analysis showed that epithelial cells undergo three stages to achieve lactation, including cellular differentiation, hormone sensing, and metabolic activation. During lactation (L0 and L20), adipocytes area accounts for less than 0.5% of mammary glands. To maintain their own survival, the adipocyte exhibited a poorly differentiated state and a proliferative capacity. Epithelial cells initiate lactation upon hormonal stimulation. After fulfilling lactation mission, their undergo physiological death under high intensity lactation. Interestingly, the physiological dead cells seem to be actively cleared by immune cells via CCL21-ACKR4 pathway. This biological process may be an important mechanism for maintaining homeostasis of the mammary gland. During natural involution (PI2 and PI7), epithelial cell populations dedifferentiate into mesenchymal stem cells to maintain the lactation potential of mammary glands for the next lactation cycle.

Conclusion: The molecular mechanisms of dedifferentiation, proliferation and redifferentiation of adipocytes and epithelial cells were revealed from late pregnancy to natural involution. This cell transcriptomic profile constitutes an essential reference for future studies in the development and remodeling of the mammary gland at different stages.

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