<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-22T19:01:58Z</responseDate><request verb="GetRecord" identifier="oai:www.repository.cam.ac.uk:1810/388345" metadataPrefix="uketd_dc">https://api.repository.cam.ac.uk/server/oai/request</request><GetRecord><record><header><identifier>oai:www.repository.cam.ac.uk:1810/388345</identifier><datestamp>2025-08-20T01:42:58Z</datestamp><setSpec>com_1810_221769</setSpec><setSpec>com_1810_256062</setSpec><setSpec>col_1810_221770</setSpec></header><metadata><uketd_dc:uketddc xmlns:uketd_dc="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:uketdterms="http://naca.central.cranfield.ac.uk/ethos-oai/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/ http://naca.central.cranfield.ac.uk/ethos-oai/2.0/uketd_dc.xsd">
   <dc:title>Epithelial and immune cell dynamics in non-traditional models of mammary postnatal development</dc:title>
   <dc:identifier xsi:type="dcterms:DOI">https://doi.org/10.17863/CAM.120743</dc:identifier>
   <dc:creator>Davies, Benjamin</dc:creator>
   <uketdterms:advisor>Hughes, Kate</uketdterms:advisor>
   <dcterms:abstract>Mammary terminal duct lobular units comprise an epithelial bilayer of luminal and
myoepithelial cells. The specific contribution of each distinct epithelial compartment to
mammary postnatal development and the mammary microenvironment remains to be
elucidated. The present study aims to exploit the ovine and rabbit mammary gland to
interrogate epithelial proliferation and immune cell dynamics during mammary postnatal
development and in mastitis. These species exhibit comparable histo-anatomy to the breast,
constituting promising adjunctive non-traditional model systems. Moreover, unlike the male
mouse, the male ovine gland persists into postnatal development. This study therefore also
aims to evaluate the male ovine mammary microenvironment as a model for male
mammary biology.

Initially, luminal and myoepithelial cell proliferation was quantified during key stages of
ovine mammary postnatal development. This demonstrated that proliferation in both
compartments is highest during the neonatal stage, correlating with an allometric
prepubescent ovine mammary growth phase. A further reduction in epithelial proliferation
was observed between pregnancy and lactation. Similar investigations of the rabbit
mammary gland indicated that proliferation remains relatively consistent from gestation to
lactation, highlighting species-specific proliferation dynamics which underpin differences in
reproductive strategies. Analysis of ovine mammary involution indicated a previously
undescribed increase in cell proliferation at approximately 2 months into the involution
process. This outlines the timeline for gland establishment for subsequent pregnancies. An
epithelial response towards mastitis was observed within both the ovine and rabbit
mammary gland. In the ovine gland, epithelial proliferation increases in cases of chronic
mastitis, detected during involution, suggesting a compensatory proliferation mechanism
within the non-necrotic mammary epithelia to limit tissue damage. In contrast, clinical cases
of lactational mastitis within rabbits resulted in a decrease in epithelial proliferation. The
epithelial response to mastitis is therefore likely dependent on the severity of the infection
and the stage of mammary development at which the mastitis occurs.

The role of myoepithelial cells within the ovine mammary microenvironment and their
interactions with macrophages were then investigated. Deep tissue 3-D imaging
demonstrated that ovine mammary myoepithelial cells undergo morphological changes
during development and the microenvironment comprises a spatially and morphologically
heterogenous macrophage population, which is closely associated with the myoepithelium.
Innovative 2-D and 3-D AI-enabled image analysis pipelines were developed, which
attempted to isolate and segregate macrophages based on their association with the
myoepithelial compartment. Whilst the difficulties in conducting 3-D image segmentation
are exemplified, the 2-D image analysis pipeline analysed a dense macrophage population
from an in-situ image and segmented individual cells to quantify their convoluted
morphology, demonstrating no significant difference in morphology between myoepithelial-associated and non-myoepithelial-associated macrophages.

Thirdly, enzymatic tissue digestion and flow cytometry protocols were successfully optimised
for ovine mammary tissues and used to investigate the impact of ovine obesity on the
pregnant mammary microenvironment. This investigation demonstrated the viability of
using ovine mammary tissue for single cell analytical techniques. Interestingly, the
proportions of mammary cell populations were unaffected by ovine obesity.

Finally, the male ovine mammary gland was explored to facilitate the understanding of
normal male mammary biology in a species in which the male gland persists postnatally.
Both intact and neutered male sheep were analysed to highlight how the male-specific sex
hormonal milieu impacts the mammary microenvironment. Irrespective of neutered status,
the male gland displays limited expression of proliferative and apoptotic markers. Up to 72%
of the luminal epithelial cells exhibit androgen receptor expression, which is significantly
abrogated by neutering. Macrophages, T-lymphocytes and mast cells were demonstrated to
cluster around the mammary ducts, implicating them in a protective immunological role
within the male gland. Neutered males also exhibit a reduction in mast cell abundance,
when compared to intact males, suggesting that hormone receptor signalling influences
mast cell recruitment.

In summary, this thesis provides insights into epithelial and immune cell dynamics to
develop our understanding of mammary development and the microenvironment. Through
utilising sheep and rabbit tissue, the data presented is more translatable to humans and
elevates the use of non-traditional mammary gland models for the breast. It further
uncovers key information that could improve animal welfare and agricultural production.</dcterms:abstract>
   <uketdterms:institution>University of Cambridge</uketdterms:institution>
   <dcterms:issued>2024-11-07</dcterms:issued>
   <dc:type>Thesis</dc:type>
   <uketdterms:qualificationlevel>Doctoral</uketdterms:qualificationlevel>
   <uketdterms:qualificationname>Doctor of Philosophy (PhD)</uketdterms:qualificationname>
   <dc:language>eng</dc:language>
   <dcterms:isReferencedBy xsi:type="dcterms:URI">https://www.repository.cam.ac.uk/handle/1810/388345</dcterms:isReferencedBy>
   <uketdterms:embargotype>embargo</uketdterms:embargotype>
   <uketdterms:embargodate>2026-08-19</uketdterms:embargodate>
   <dc:identifier xsi:type="dcterms:URI">https://www.repository.cam.ac.uk/bitstreams/873b4ed8-c455-4191-bde8-165a8f5f8c79/download</dc:identifier>
   <uketdterms:checksum xsi:type="uketdterms:MD5">9774dbd800c207ab1fb3619e3397526e</uketdterms:checksum>
   <dcterms:license>https://www.repository.cam.ac.uk/bitstreams/6adaa01b-956e-4fca-a384-cc6217e8cf6a/download</dcterms:license>
   <uketdterms:checksum xsi:type="uketdterms:MD5">87eda9de84448d1f82354d60eee3eb5f</uketdterms:checksum>
   <dc:rights>http://purl.org/NET/rdflicense/allrightsreserved</dc:rights>
   <dc:subject>Mammary Gland</dc:subject>
   <dc:subject>Postnatal Development</dc:subject>
   <dc:subject>Myoepithelial Cell</dc:subject>
   <dc:subject>Macrophage</dc:subject>
   <dc:subject>Ovine</dc:subject>
   <dc:subject>Rabbit</dc:subject>
   <dc:subject>Male Mammary Biology</dc:subject>
   <dc:subject>Epithelial Cell</dc:subject>
   <dc:subject>Microenvironment</dc:subject>
   <dc:subject>Model</dc:subject>
</uketd_dc:uketddc>
</metadata></record></GetRecord></OAI-PMH>