The mammary gland represents a unique tissue to study organogenesis as it predominantly develops in the post-natal animal and undergoes dramatic morphogenetic changes during puberty and the reproductive cycle. The physiological function of the mammary gland is to produce milk to sustain the newborn. Here we view the lactating gland through three-dimensional confocal imaging of intact tissue. We observed that the majority of secretory alveolar cells are binucleated. These cells first arise in very late pregnancy due to failure of cytokinesis and are larger than mononucleated cells. Augmented expression of Aurora kinase-A and Polo-like kinase-1 at the lactogenic switch likely mediates the formation of binucleated cells. Our findings demonstrate an important physiological role for polyploid mammary epithelial cells in lactation, and based on their presence in five different species, suggest that binucleated cells evolved to maximize milk production and promote the survival of offspring across all mammalian species.
The overall structure of an organ is dictated by the shape, size and arrangement of its constituent cells. The mammary gland is a remarkably adaptive organ that offers a unique model to understand how an organ changes its structure to meet its physiological requirements. Post-natal development of the mammary gland occurs through distinct stages, encompassing puberty, pregnancy, lactation and involution, each of which involves drastic changes in tissue architecture1,2. Ductal morphogenesis in puberty culminates in the generation of a highly elaborate bilayered ductal tree comprising cells of the luminal and myoepithelial lineages. During pregnancy, the number of epithelial cells increases exponentially, with the formation of alveolar luminal units that differentiate in late pregnancy. Labelling assays have indicated that cell proliferation rapidly declines after mid-pregnancy as the gland commits to differentiation, and that a synchronized round of DNA synthesis occurs in early lactation3,4,5.
When alveolar epithelial cells enter the secretory activation phase in late pregnancy, they accumulate endoplasmic reticulum and golgi, and become enlarged through the production of milk. Milk contains several nutritional components for the newborn, including milk proteins, lipids and carbohydrates6,7. At the switch to lactation, the outer myoepithelial cells contract in response to oxytocin to expel milk from the alveolar luminal cells. Understanding the tissue remodelling processes that underlie the formation of the specialized milk-producing alveoli requires a comprehensive view of the cellular structure of the mammary gland.
In this report, we have applied three-dimensional (3D) imaging technology to provide a unique view of the mouse mammary gland and uncovered the presence of a large population of binucleated alveolar cells in lactation. These cells first appear in late pregnancy owing to failed cytokinesis rather than cell fusion. Mechanistically, we show that Aurora kinase-A (AURKA) and Polo-like kinase-1 (PLK-1) likely control the generation of binucleated cells at the switch to lactation, in response to signals that include prolactin and epidermal growth factor (EGF). The binucleated alveolar state was shown to be essential for effective lactation. Pertinently, polyploid cells were readily identified in the lactating mammary glands of four other mammalian species (human, cow, seal and wallaby), implying that polyploidy is an evolutionarily conserved mechanism to enable successful lactation. Our findings that binucleated cells are required for lactation represent one of the few physiological functions ascribed to polyploid mammalian cells thus far.
A novel population of binucleated alveolar cells in lactation
We previously developed a high resolution 3D confocal imaging technique to visualize expansive regions of intact tissue (up to 1 cm) at single-cell resolution8. Using this technology to study mammary gland architecture, we surprisingly unveiled a substantial fraction of binucleated luminal cells (E-cadherin+) in the lactating mammary gland (Fig. 1a, Supplementary Fig. 1a and Supplementary Movie 1). Although an early dissertation reported the presence of binucleated cells in lactation9, this observation was considered to possibly represent an artefact of tissue fixation10 and no further evidence for this phenomenon has been described over decades. This largely reflects the limitations of two-dimensional microscopy, where it is difficult to visualize cells in their native state, particularly in densely packed tissue such as the lactating mammary gland, thus necessitating the use of 3D confocal imaging. While a majority of binucleated luminal cells was readily identifiable in the lactating gland by this technology, these cells were not detectable on day 16.5 of pregnancy (Fig. 1b) but appeared by day 18.5 when the gland has entered the secretory phase (Supplementary Fig. 1b)6. No cells containing more than two nuclei were observed, indicating that this process is strictly regulated. Myoepithelial cells, resident in the sheath around the alveolar luminal cells, remained mononucleated at all stages of development. Immunostaining at 4 days of lactation indicated that binucleated cells expressed abundant milk protein (Supplementary Fig. 1a). At 18.5 days of pregnancy, the nuclei and organelles were localized to the cell periphery on either side of the large cytoplasmic lipid droplet that characterizes cells at this stage (Supplementary Fig. 2a,b). Curiously, the size and location of this droplet changes after parturition such that large lipid droplets are replaced by small droplets localized to the apical surface of alveolar cells6. Thus, in lactating tissue, the nuclei and organelles are positioned within the central area of the alveolar cells (Supplementary Fig. 2c).
Following the cessation of lactation, the number and differentiation status of epithelial cells returns to their pre-pregnant state11. Involution is an essential process to remove milk-producing cells that are no longer required and is executed through large-scale programmed cell death. Notably, binucleated cells appear highly susceptible to cell death and are rapidly cleared within the first 48 hours of involution by apoptosis (Supplementary Fig. 3c,b), as indicated by the presence of binucleated cells positive for cleaved caspase-3 (CC3). No CC3+ cells were evident in lactation, as expected (Supplementary Fig. 3a,b). Efficient apoptosis of polyploid cells during involution is envisaged to be crucial for returning the gland to its pre-pregnant state in order to avert cell transformation of polyploid cells that might occur in response to hormonally-driven oestrus cycling. Indeed, genome duplication has been shown to promote neoplastic transformation of mammalian cells12,13.
Increased DNA ploidy of alveolar cells from late pregnancy
To establish the DNA ploidy of cells during pregnancy and lactation, we performed flow cytometric analysis of three different cell populations: the luminal (Lin–CD29loCD24+), stem cell-enriched basal (Lin–CD29hiCD24+) and stromal (Lin–CD24–) subsets14. At 16.5 days of pregnancy, only a small proportion of alveolar luminal cells contained a 4N DNA content by flow cytometry (Fig. 1c). The proportion of these cells increased dramatically from ∼17% at 18.5 days of pregnancy to ∼50% at 2 days of lactation (Fig. 1c,d). The higher proportion of binucleated cells apparent by confocal analysis (Fig. 1a) presumably reflects the fragility of these cells, which can be lost during tissue dissociation. In contrast to the luminal compartment, the basal and stromal populations contained a small subset of cells (<8%) with a DNA content of 4N in pregnancy and lactation. To address the cycling status of mammary epithelial cells at 16.5 versus 18.5 days of pregnancy, Hoechst-stained cell populations were analysed by flow cytometry. A comparable percentage of cells exhibited a 4N DNA content (12.5 versus 17.4% at 16.5 and 18.5 days of pregnancy, respectively) (Supplementary Fig. 4). However, binucleated cells were only apparent at 18.5 days of pregnancy based on confocal analysis of sorted cells with either a 2N or 4N DNA content (Supplementary Fig. 4). Thus, the 4N peak at 18.5 days pregnancy (dP) represents cells in the binucleated state plus cells in the G2/M phase of the cell cycle, whereas the 4N peak at 16.5 days corresponds to cells in G2/M.
Larger cell volume conferred by the binucleated state
We next performed a volumetric analysis of alveolar luminal cells from late pregnant and lactating mammary glands. In order to capture quantitative information from our complex 3D imaging data (up to 150 GB per image), we established a semi-automated technique (see Methods). Substantially greater volumes were observed for binucleated compared with mononucleated cells (Fig. 1e–g), but the sizes of individual nuclei were comparable. Notably, the overall cell volume increased substantially from late pregnancy to 4 days of lactation but plateaued after this time (Fig. 1g).
Polyploid cells arise through failed cytokinesis
To explore potential mechanisms involved in the production of binucleated alveolar cells, we considered either cell fusion or failed cytokinesis. By exploiting the multi-colour confetti system15 combined with a doxycycline-inducible cre under the control of the Elf5 promoter, we first examined whether a fusion mechanism might account for the formation of binucleated cells. Elf5 is exclusively expressed in luminal progenitor cells in the virgin gland8 and the vast majority of luminal cells in the pregnant gland16. The confetti reporter locus was triggered in late pregnancy (15.5 days) in Elf5-rtTA/TetO-cre/R26R-Confetti mice to randomly activate the expression of one of its four colours, and scanned for the presence of multi-coloured cells at 4 days of lactation. No double-labelled cells were apparent, indicating that cell fusion had not occurred (Fig. 2a), such as occurs in the case of skeletal muscle cells.
We next turned to EdU-labelling studies to address cell division. Pregnant dams at 16.5 or 18.5 dP were injected with a single dose of EdU and subjected to 3D confocal imaging after a defined chase period. At 16.5 days, only dividing mononucleated cells were evident at 6 h after EdU injection. In contrast, at 18.5 days, binucleated EdU+ luminal cells appeared after a 6 h chase, with an abundance of these cells evident after analysis at 3 days (Fig. 2b). These data suggest that some alveolar cells can execute DNA replication in very late pregnancy but fail to undergo cytokinesis to produce two cells for lactation. Pulse-chase experiments in which mice were injected with EdU on day 18.5 of pregnancy and then analysed 3 and 12 days later showed that binucleated EdU+ cells are relatively long lived for highly metabolic cells (Fig. 2c). Analysis of the distribution of EdU+ cells in mono- versus bi-nucleated cells confirmed the shift towards binucleation at the onset of lactation (Fig. 2d). There are fewer EdU+ mononucleated cells in lactation compared with 18.5 days of pregnancy as these cells undergo one further round of division (with aborted cytokinesis) to generate cells comprising two nuclei.
AURKA and PLK-1 are upregulated at the lactation switch
To interrogate possible genes that govern the balance between mononucleated and binucleated cells at the onset of lactation, we examined the RNA-seq expression profiles of genes differentially expressed between late pregnancy and early lactation in luminal cells17. Aurora kinase A (AURKA) emerged as one of the top hits upon analysis of upregulated genes in the cell cycle functional group (Fig. 3a). AURKA encodes a mitotic spindle-associated kinase that coordinates the functions of centrosomes, spindle formation and kinetochores required for mitotic progression and genomic integrity18. Quantitative PCR with reverse transcription (qRT–PCR) (Supplementary Fig. 5a) and western blot analysis (Fig. 3b) of sorted cells showed that AURKA was markedly upregulated in the luminal cell compartment at the onset of lactation relative to levels in late pregnancy. As anticipated, no change in AURKA protein levels was observed in the basal cell population. Evaluation of protein expression during lactation revealed that AURKA levels were high at the onset of lactation but declined to undetectable levels by day 4 (Supplementary Fig. 5b), suggesting that AURKA only functions around the lactation switch.
We next addressed the expression of other signalling kinases that are critical for cytokinesis, PLK-1 and AURKB18,19. PLK-1, a substrate of AURKA, was also markedly upregulated in early lactation relative to late pregnancy based on RNA-seq analysis (Fig. 3a), while no change was evident in AURKB expression, as confirmed by qRT–PCR analysis (Supplementary Fig. 5a). In summary, these data implicate the mitotic kinases AURKA and PLK-1 in the regulation of cytokinesis at the lactational switch.
Given that prolactin (Prl) is a key lactogenic hormone20,21, we explored whether Prl could induce AURKA expression and binucleation in vivo by treating mice for 3 days with Prl during late pregnancy (from 15.5 to 17.5 days), followed by analysis 6 h post-injection on day 17.5. Analysis of mammary glands showed a very low proportion of binucleated cells, implying that Prl alone is not sufficient to induce this process (Supplementary Fig. 6a,b). Since EGF is dramatically induced at the onset of lactation17, we next treated mice with a combination of Prl and EGF over the same time course. Strikingly, we observed the induction of binucleated cells (∼30%) concomitant with induction of AURKA by western blot analysis (Supplementary Fig. 6). Thus, Prl and EGF form part of the signal that instructs alveolar cells not to undergo cytokinesis in early lactation, thus leading to a binucleated cellular state.
AURKA is essential for the formation of binucleated cells
To investigate whether AURKA plays a role in the formation of binucleated cells, we first conditionally deleted this gene using the WAP-icre strain that drives cre expression in differentiated alveolar cells from late pregnancy. Fluorescence-activated cell sorting (FACS) analysis and confocal imaging in 3D demonstrated that loss of AURKA profoundly disrupted the generation of binucleated cells at the onset of lactation. Only mononucleated cells were evident in 3D images of AURKA-deficient glands, with a greater than five-fold decrease in the number of cells with a 4N DNA content evident by FACS analysis (Fig. 3c,d and Supplementary Fig. 7a). Moreover, there was substantially less milk protein in these glands compared with that in control dams (Fig. 3d), and examination of pups nursed by WAP-icre/AURKAf/f dams revealed severe stunting of pups compared with those nursed by AURKAf/f or WAP-icre/AURKAf/+ dams (Fig. 3e). qRT–PCR analysis confirmed drastically lower levels of α-casein, β-casein and WAP gene expression in AURKA-deficient glands (Supplementary Fig. 7b), while western blotting validated deletion of AURKA (Fig. 3f). Importantly, EdU labelling at P0 after doxycycline-mediated deletion of AURKA showed the presence of EdU+ cells in AURKA-deficient glands (Supplementary Fig. 7c), indicating that cells could enter S phase and undergo DNA replication. This observation is compatible with a specific role for AURKA in the lactating mammary gland in the regulation of cytokinesis.
We next turned to a more sophisticated cre recombinase system to temporally delete the AURKA gene in late pregnancy versus early lactation utilizing a doxycycline-inducible cre under the control of the Elf5 promoter8. Elf5 is a master transcriptional regulator of the secretory alveolar lineage16 and is highly expressed in luminal cells of pregnant and lactating mammary glands (Supplementary Fig. 8a). Evaluation of lactating mammary glands from Elf5-rtTA/TetO-cre/AURKAf/f dams by 3D confocal imaging and FACS analysis showed a marked decrease in the proportion of binucleated cells relative to control Elf5-rtTA/AURKAf/f dams at 2 days of lactation, following treatment with doxycycline from day 16.5 of pregnancy (Fig. 4a and Supplementary Fig. 8b). Notably, FACS analysis of control Elf5-rtTA/AURKAf/f glands indicated that almost all binucleated cells (>98%) expressed Elf5 (Supplementary Fig. 8b,c). AURKA-deficient glands also exhibited a dramatic decline in milk production, resulting in impaired lactation and the stunted growth of pups (Fig. 4a–c). For both the Elf5/TetO-cre and WAP-icre-driven models, 20–30% of pups in some litters were found to die around day 10 of lactation owing to insufficient milk production by AURKA-deficient mothers. A lower density of alveolar units persisted in these mammary glands on day 14 of lactation relative to both control and heterozygous glands (phenotypically normal) (Supplementary Fig. 9a–c). By contrast, doxycycline treatment from days 1 or 4 of lactation, when binucleated cells have already been generated, had no effect on lactogenesis or histology (Fig. 4d,e and Supplementary Fig. 9d). Induction of deletion from P0 resulted in a small decrease in lactogenic capacity and pup weight, although the histology of the glands appeared normal (Supplementary Fig. 9e).
Inhibition of AURKA or PLK-1 activity prevents binucleation
In addition to targeted deletion, we examined the effects of pharmacological inhibition of AURKA or PLK-1 on the formation of binucleated cells. Mice were treated with either the AURKA (MLN8237) or PLK-1 (BI6727) inhibitor, which directly inhibit kinase activity, or vehicle from 16.5 days of pregnancy and then mammary glands isolated from these mice were assessed at 2 days of lactation. FACS analysis showed a greater than twofold decrease in the proportion of alveolar cells with 4N DNA content by either inhibitor (Fig. 5a,b), while confocal 3D imaging revealed a predominance of mononucleated cells (Fig. 5c,d). No change was evident in the DNA ploidy of basal or stromal cells, thus serving as a control (Fig. 5a). These data also indicate that mitosis was not blocked upon inhibition of these mitotic kinases near the lactation switch, and thus does not account for the lack of binucleation. Furthermore, pups lacked milk in their stomachs, indicating that lactogenesis was impaired. These results are consistent with the notion that the increase in expression/activity of AURKA and PLK-1 occurring at the onset of lactation is critical for preventing cytokinesis and the formation of binucleated cells.
Conservation of polyploid cells across mammalian species
Given that polyploidy is essential for maximal lactogenesis in the mouse, we speculated that it might be a feature of other mammalian species. To this end, we examined lactating tissue from human breast, seal and wallaby, and of late pregnant tissue from cow. As binucleated cells are not readily detectable in two-dimensional sections, we performed 3D confocal microscopy on thick tissue sections (up to 400 μm) from paraffin or OCT blocks using a modification of the procedure for whole-mounted fresh tissue. Fresh human tissue was also assessed, yielding similar findings. Remarkably, binucleated cells were prominent in all species examined, with ∼30% observed in human, seal and wallaby tissue, and 40% in bovine mammary tissue (Fig. 6a–e and Supplementary Fig. 10).
Through the use of 3D confocal imaging, our studies have uncovered the presence of remarkable numbers of polyploid alveolar cells in the lactating mouse mammary gland. These cells arise through a blockade in cytokinesis and have a considerably larger volume than cells comprising a single nucleus. Moreover, they play an essential role in lactogenesis. During lactation, the sole function of alveolar epithelial cells is to generate large amounts of milk protein, lipid and carbohydrate, to support the offspring6. Polyploid cells presumably evolved around the onset of lactation to enhance milk production. The larger cytoplasmic volume of binucleated alveolar cells likely accommodates more ribosomes, ER and Golgi required for the biosynthesis of milk protein and lipid22. In addition, these larger cells have a greater apical surface area to enable more efficient milk secretion.
Mechanistically, the mitotic kinases AURKA and PLK-1 have emerged as key regulators of cytokinesis of mammary alveolar cells at the lactogenic switch. The function of AURKA is not only pivotal to centrosome function and mitotic assembly18,19, but there is emerging evidence to suggest that it is implicated in the early stages of cytokinesis23,24,25. The two lactation-specific AURKA knockout models explored here highlight the importance of binucleated alveolar cells for efficient milk production and lactation. Only deletion of AURKA at the switch to lactation inhibited the formation of binucleated cells and milk synthesis. These findings underscore the importance of timing of expression of this serine/threonine kinase. Moreover, the precise level of AURKA expression has been shown to be crucial for proper cytokinesis, where inhibition26 or overexpression27,28,29 of this gene resulted in failed cytokinesis and the formation of binucleated cells. Pertinently, AURKA is frequently amplified in breast cancer, and overexpression of this gene in mouse genetic models accelerates oncogenesis by inducing genetic instability and the formation of binucleated cells, which succumb to apoptosis29,30. In a physiological setting, our findings uncover an important role for AURKA in the generation of polyploid milk-producing cells at the switch to lactation.
Inhibition of PLK-1, a substrate of AURKA and an important regulator of cytokinesis19, also led to a block in cytokinesis at the lactational switch. These data recapitulate those seen upon genetic ablation or pharmacological inhibition of AURKA, suggesting that control of cytokinesis in lactation is a shared function of these kinases. Overexpression of PLK-1 has been previously reported to cause multinucleation and interfere with cytokinesis28, emphasizing the importance of the absolute levels of mitotic kinases in control of the cell cycle. Together, these data suggest that augmented expression (and activity) of these two kinases, specifically at the onset of lactation, is key to the prevention of cytokinesis after chromosome segregation and nuclear division. In the mammary gland, moderate levels of AURKA and PLK-1 are presumably required for mitotic progression, whereas increased levels of these kinases at a specific temporal window trigger a failure of cytokinesis to enable the production of binucleated alveolar cells in lactation.
Polyploidy has been demonstrated to be a feature of specific mammalian cell types including the megakaryocyte, hepatocyte, trophoblast giant cell and cardiomyocyte31,32. These cells differ in their function and number of chromosome sets, and although it is presumed that polyploidy confers a considerable advantage on tissue growth or differentiation, its functional significance is poorly understood. There is evidence to suggest that polyploidy may be important for cardiac muscle under stress conditions, since mice lacking a gene necessary for polyploidy were normal at baseline but their hearts pumped substantially less blood after an infarct33. Similarly, the high proportion of polyploid cells in the liver may be required to mediate a proper stress-response34. In the mammary gland, which evolved as an epidermal appendage over 300 million years ago, we demonstrate a crucial role for polyploidy in enabling effective lactation. Our data further suggest that polyploid alveolar cells evolved as a conserved feature in lactation to support the nutritional requirements of the young across all mammalian species.
AURKAf/f mice35 were obtained from the Jackson Laboratory. WAP-icre36, TetO-cre37 and R26R-Confetti mice15 were kind gifts from G. Schuetz (German Cancer Research Centre, Heidelberg), K. Schönig (Central Institute of Mental Health, Mannheim) and H. Clevers (Hubrecht Institute, Utrecht), respectively. Elf5-rtTA-GFP mice were generated at the Walter and Eliza Hall Institute of Medical Research (WEHI)8. FVB/N mice were provided by the animal facility of WEHI. All mice were bred and maintained in our animal facility according to the institutional guidelines, and all experiments were approved by the WEHI Animal Ethics Committee.
For timed pregnancies, adult female mice were mated with FVB/N stud males, scored by the presence of a vaginal plug and confirmed by the examination of embryos at the time of mammary gland collection. For lactation experiments, adult female mice were mated with FVB/N stud males and six offspring per litter were maintained. For in vivo EdU (5-ethynyl-2-deoxyuridine; Invitrogen) label, mice were injected intraperitoneally (IP) with 0.2 mg of EdU (200 μl, 1 mg ml−1 in PBS). For induction of deletion of AURKA in the Elf5-rtTA/TetO-cre/AURKAf/f line, mice were administered doxycycline via food pellets8 from 16.5 days of pregnancy (dP), or 0 (birth), 1 or 4 days lactation (dL) until collection of mammary glands for analysis to ensure efficient deletion. For induction of expression of the Confetti reporter in the Elf5-rtTA/TetO-cre/R26R-ConfettiKI/+ line, mice were injected IP (once) with 2 mg of doxycycline (100 μl, 20 mg ml−1 in PBS; Sigma) at 15.5 days of pregnancy. To inhibit the kinase activity of AURKA and PLK-1 kinase, MLN8237 (1.25 mg per mouse, daily) or BI6727 (0.75 mg per mouse, daily) were administered, respectively, via oral gavage to pregnant mothers from 16.5 dP to 1dL and mice were collected and analysed at 2 days of lactation. To test the effect of prolactin/EGF on the generation of binucleated cells, pregnant mothers were subcutaneously injected with prolactin (0.2 mg per mouse, twice per day) with or without IP injection of EGF (0.01 mg per mouse, twice per day) between 15.5 and 17.5 dP. Mice were then collected and analysed 6 h after the last injection.
Human breast tissue
Human breast tissue was obtained from consenting individuals through the Victorian Cancer Biobank with approval from the Human Research Ethics Committee of The Walter and Eliza Hall Institute of Medical Research. Fresh samples were normal breast tissue (confirmed by pathology) from reduction mammoplasties. Three paraffin-embedded (PE) and two fresh samples were analysed.
Mammary cell suspension preparation and flow cytometry
Mammary glands were dissected from adult female mice, and single-cell suspensions were prepared14. To assess ploidy through measuring DNA content, cells were first incubated with 20 μg ml−1 Hoechst 33342 (Invitrogen) at 37 °C shaker for 1 h and maintained in a solution containing 20 μg ml−1 Hoechst 33342 in all steps after staining to prevent the release of dye from the cells. Otherwise, cells were directly stained with antibodies on ice for 25 min. The following antibodies were used: PE anti-mouse CD24 (rat, clone M1/69, BD; 1:200 dilution), APC/cy7 anti-mouse/rat CD29 (rat, clone HMb1-1, BD; 1:200 dilution), APC anti-mouse CD45 (rat, clone 30-F11, BD; 1:100 dilution), APC anti-mouse Ter119 (rat, clone Ter-119, BD; 1:100 dilution) and APC anti-mouse CD31 (rat, clone MEC13.3, BD; 1:50 dilution). Cells were re-suspended in 4 μg ml−1 7-AAD (Sigma) before analysis to exclude dead cells. FACS analysis and sorting were performed using a FACS LSRIIC and an Aria (Becton Dickinson), respectively. The Lin– population was defined as Ter119–CD31–CD45– (ref. 14). FACS data were analysed using FlowJo software (Tree Star).
Whole mounting and histology of mammary glands
For whole-mount analysis, mammary glands were fixed in Carnoy’s solution containing ethanol, chloroform and glacial acetic acid (6:3:1) at room temperature for 48 h before staining with carmine alum. Mouse mammary glands were fixed in 4% paraformaldehyde, embedded in paraffin, sectioned and then stained with haematoxylin and eosin.
Western blot analysis
FACS-sorted cells were directly lysed in RIPA buffer containing 1 × complete mini protease inhibitor cocktail (Roche) and 1 × Roche PhosSTOP phosphatase inhibitor cocktail (Roche). Whole mammary gland lysates were prepared by grinding tissue in liquid nitrogen and solubilizing in the RIPA buffer. The following primary antibodies were used for western blot analysis: anti-AURKA (mouse, clone 4/IAK1, BD; 1:500 dilution) and anti-beta-Actin (mouse, clone AC-15, Sigma; 1:5,000 dilution). All uncropped Western blots can be found in Supplementary Fig. 11.
RNA preparation and quantitative RT–PCR analysis
Total RNA was prepared using the RNeasy Micro kit (Qiagen) from FACS-sorted luminal cells isolated from the mammary glands of FVB/N dams at 18.5 dP or 2 days of lactation, or from total mammary tissue derived from AURKA-deficient or control mice at 14 days of lactation. Reverse transcription was carried out using oligo(dT) primer and SuperscriptIII reverse transcriptase (Invitrogen, MA, USA). Quantitative RT–PCR analysis was performed using a Rotorgene RG-6000 (Corbett Research, Australia) and normalized against 18S ribosomal RNA.
Whole-mount preparation of fresh tissue for 3D confocal imaging
Tissues were fixed in 4% paraformaldehyde and incubated overnight at 4 °C with primary antibodies. The following day, tissues were incubated with secondary antibodies, DAPI and phalloidin. Tissues were subsequently incubated in 80% glycerol before dissection for 3D imaging, as previously described8. The following primary antibodies were used for 3D confocal imaging: anti-E-cadherin (rat, clone ECCD-2, Invitrogen; 1:200 dilution), anti-Keratin 5 (rabbit, Covance; 1:500), anti-β-catenin (mouse, Cell Signaling; 1:500), anti-Milk (Accurate Chemical and Scientific Corporation; 1:1,000), anti-giantin (rabbit, Abcam; 1:250), cleaved caspase-3 (rabbit, clone D3E9, Cell Signaling; 1:100 dilution) and anti-GFP (chicken, Abcam; 1:500). Secondary antibody: Alexa Fluor (Invitrogen; 1:500). F-actin was stained with Alexa Fluor 647 Phalloidin (Invitrogen; 1:50 dilution). DAPI (Invitrogen) was used at 1 μg ml−1. EdU labelling was performed using the Click-it kit (Invitrogen).
Preparation of embedded mammary tissue for confocal microscopy
Collection of mammary tissue from the cow, tammar wallaby (Macropus eugenii) and cape fur seal (Arctocephalus pusillus pusillus) is described elsewhere38,39,40. Three lactating mammary tissues embedded in OCT (Optimal Cutting Temperature) were analysed for seal; one paraffin-embedded (PE) and two OCT-embedded lactating samples were analysed for wallaby; three PE bovine specimens from late pregnancy were analysed. Human tissue was either fresh or PE (n=5). For 3D imaging, we prepared thick sections (up to 400 μm) using a microtome (Leica RM2) and then dewaxed using conventional procedures41. An antigen retrieval step was then performed in DAKO Target Retrieval pH9 solution at 90 °C for 30 min. OCT-embedded floating sections were cut using a cryostat (Microm HM550, Thermo Scientific) and then fixed in 4% paraformaldehyde for 30 min before immunostaining according to Rios et al.8.
Imaging quantification for cell volume analysis
We performed cell volume measurements using the surface module in Imaris and binary masks produced from a segmentation process developed in FIJI. The segmentation method involved filtering, thresholding and inverting the [MEMBRANE STAIN/CHANNEL] and running a watershed algorithm seeded with points furthest from all membranes. The resulting particles were filtered for size to remove any clearly incorrect regions. The segmentation was manually validated on a slice-by-slice basis via a user-interface allowing selection of individual cells, where the segmentation was consistent with the cell morphology and staining. Any missing slices (or slices that were clearly incorrect) were filled in by interpolating between the two nearest slices assessed to be accurate. Once cell selection and validation had been performed, a binary mask of only the cells of interest was imported into Imaris for the volume measurements. Approximately 50 cells were analysed per mouse (n=3) at each time-point.
Imaging quantification of nuclei
The module cell counter from Image J was used to count the number of cells with one or two nuclei in 3D images.
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We are very grateful to J. Petersen and C. Ormandy for discussions, F. Jackling, M. Le Page, J. Szarlat, K. Liu, J. Sharp, F. Vaillant and A.T.L. Lun for expert assistance and the Animal, FACS, Imaging and Histology facilities at WEHI and to the Victorian Cancer Biobank (supported by the Victorian State Government), which provided coded breast tissue. This work was supported by the Australian National Health and Medical Research Council (NHMRC) grants #1016701, #1085191 and #1086727; NHMRC IRIISS; the Victorian State Government through Victorian Cancer Agency funding and Operational Infrastructure Support; and the Australian Cancer Research Foundation. A.C.R. and N.Y.F. were supported by a National Breast Cancer Foundation (NBCF)/Cure Cancer Australia Fellowship; G.J.L. by a NHMRC Fellowship #1078730 and J.E.V. by an Australia Fellowship #1037230.
The authors declare no competing financial interests.
Supplementary Figures 1-11 (PDF 15343 kb)
Animation made with the Imaris software showing a three dimensional reconstruction of a ductal tree portion (volume 1.8 mm3) from a FVB/N mouse at 2 days of lactation. The whole-mount was labelled with DAPI (white), E-cadherin (green) and F-actin (red). (MOV 18513 kb)
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Rios, A., Fu, N., Jamieson, P. et al. Essential role for a novel population of binucleated mammary epithelial cells in lactation. Nat Commun 7, 11400 (2016). https://doi.org/10.1038/ncomms11400
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