Abstract

Bovine mammary function at molecular level is often studied using mammary tissue or primary bovine mammary epithelial cells (pbMECs). However, bulk tissue and primary cells are heterogeneous with respect to cell populations, adding further transcriptional variation in addition to genetic background. Thus, understanding of the variation in gene expression profiles of cell populations and their effect on function are limited. To investigate the mononuclear cell composition in bovine milk, we analyzed a single-cell suspension from a milk sample. Additionally, we harvested cultured pbMECs to characterize gene expression in a homogeneous cell population. Using the Drop-seq technology, we generated single-cell RNA datasets of somatic milk cells and pbMECs. The final datasets after quality control filtering contained 7,119 and 10,549 cells, respectively. The pbMECs formed 14 indefinite clusters displaying intrapopulation heterogeneity, whereas the milk cells formed 14 more distinct clusters. Our datasets constitute a molecular cell atlas that provides a basis for future studies of milk cell composition and gene expression, and could serve as reference datasets for milk cell analysis.

Highlights

  • Background & SummaryBovine mammary structure, function, development and immune response and the underlying transcriptional regulatory processes in the mammary tissue have been studied extensively for almost half a century

  • Bovine mammary gland tissue can only be collected by biopsy or after slaughter, and comprises a number of heterogeneous cell types (e.g., mammary epithelial cells (MECs), myoepithelial cells, adipocytes, fibroblasts) creating potential bias in the outcome of global transcriptome analyses depending on cell composition

  • Another specific feature of mammary gland tissue is the low complexity of its transcriptome, because milk and whey protein genes are highly expressed, in consequence masking the expression of lowly expressed transcripts[3,4]

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Summary

Background & Summary

Function, development and immune response and the underlying transcriptional regulatory processes in the mammary tissue have been studied extensively for almost half a century. Bovine mammary gland tissue can only be collected by biopsy or after slaughter, and comprises a number of heterogeneous cell types (e.g., mammary epithelial cells (MECs), myoepithelial cells, adipocytes, fibroblasts) creating potential bias in the outcome of global transcriptome analyses depending on cell composition Another specific feature of mammary gland tissue is the low complexity of its transcriptome, because milk and whey protein genes are highly expressed, in consequence masking the expression of lowly expressed transcripts[3,4]. Recent technical advances allow transcripts from thousands of cells to be pooled, sequenced, and subsequently identified in a single experiment at single-cell resolution[16] This approach enables to assess the functional heterogeneity in a cell sample by identifying and characterising subpopulations of cells in a complex cell population[17,18,19]. They provide a suitable reference and basis for future single-cell gene expression studies, e.g., to investigate the response of specific cells to environmental disruptors including pathogen challenges

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