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A cell transcriptomic profile p ovides insights into adipocytes of porcine mammary gland across developmentOACSTPCD

中文摘要

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.

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;

State Key Laboratory of Swine and Poultry Breeding Industry,College of Animal Science and Technology,Sichuan Agricultural University,Chengdu 611130,China Key Laboratory of Qinghai‑Tibetan Plateau Animal Genetic Resource Reservation and Utilization,Southwest Minzu University,Chengdu 610041,ChinaState Key Laboratory of Swine and Poultry Breeding Industry,College of Animal Science and Technology,Sichuan Agricultural University,Chengdu 611130,ChinaAnimal Breeding and Genetics Key Laboratory of Sichuan Province,Sichuan Animal Science Academy,Chengdu 610000,ChinaKey Laboratory of Qinghai‑Tibetan Plateau Animal Genetic Resource Reservation and Utilization,Southwest Minzu University,Chengdu 610041,China Animal Breeding and Genetics Key Laboratory of Sichuan Province,Sichuan Animal Science Academy,Chengdu 610000,China

畜牧业

AdipocytesCell–cell interactionDevelopmentMammary glandsnRNA-seq

《Journal of Animal Science and Biotechnology》 2024 (001)

P.182-200 / 19

supported by the National Key R&D Program of China (2020YFA0509500,2021YFD1301101 and 2021YFA0805903);the Sichuan Science and Technology Program;(2023YFN0088 and 2021YFYZ0030);the National Center of Technology Innovation for Pigs (SCCXTD-2023-08);the National Natural Science Foundation of China (32272837 and 32225046);Tianfu Agricultural Master Project。

10.1186/s40104-023-00926-0

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