A flow cytometric method for measuring and isolating mammary epithelial cells from bovine milk

• Published in: JDS communications 2021-11, Vol.2 (6), p.426-430
• Main Authors: Lengi, A.J., Makris, M., Corl, B.A.
• Format: Article
• Language: English
• ISSN: 2666-9102; 2666-9102
• DOI: 10.3168/jdsc.2021-0135

[Display omitted] •Flow cytometry using an antibody against butyrophilin allows quantification of mammary epithelial cells in milk.•Sorting butyrophilin-positive or CD45-negative cells isolates epithelial cells from milk.•Selection for cytokeratin was not effective in this flow cytometry application. Sampling frequent time points of mammary signaling pathways is not possible with tissue biopsies. We have validated a flow cytometry and cell sorting procedure for isolating live bovine mammary epithelial cells from somatic cell populations in milk using butyrophilin 1A1 as a marker for mammary epithelial cells and CD45 as a marker for hematopoietic cells. Hoechst 33342 staining and propidium iodide exclusion were used to select for nucleated live cells. Positive selection of butyrophilin (BTN)-expressing cells was performed by fluorescence-activated cell sorting. Quantitative real-time PCR performed on mRNA isolated from these cells showed a 226-fold increase in κ-casein (CSN3) mRNA expression in BTN single-positive cells compared with unsorted cells, whereas CD45 single-positive cells showed a significant decrease. A negative selection strategy for cells not expressing the hematopoietic cell marker CD45 also resulted in a cell population with a 196-fold increase in CSN3 mRNA expression compared with unsorted cells. We found no enrichment of CSN3 mRNA expression after sorting cells using cytokeratin antibodies. The noninvasive assays described here allow for daily or more frequent sampling time points for measurement of mammary epithelial cells during the course of lactation.