Despite long-standing interest, the cellular mechanisms driving the initiation of mammary gland development have remained elusive for decades, mostly due to technical limitations in studying dynamic cell behaviors in live tissues. Recent advances in microscopic methods and availability of various mouse models allowed the research group of Marja Mikkola from HiLIFE Institute of Biotechnology, University of Helsinki to address this question. This is the first time when live tissue imaging has been used to visualise the emergence of the mammary gland.
Mammary gland is the class-defining organ of mammals, yet we know surprisingly little how its development commences. In their recent study published in Journal of Cell Biology,
“Interestingly, mammary bud cells, unlike most of other skin derivatives such as hair follicle and tooth bud, do not divide for several days, indicating that this might be a unique feature of early mammary gland development” says graduate student
Mammary buds use a previously undescribed mechanism for invagination
Tissue invagination, or tissue folding inwards into the underlying stroma, is a fundamental mechanism that occurs to generate the architecture of many organs. In the same piece of work, the authors describe a novel mechanism for tissue invagination.
“Using confocal fluorescence microscopy, we found thin and elongated epidermal keratinocytes surrounding mammary bud in a rim like fashion: their appearance and disappearance coincided with the invagination process suggesting that these cells, named ring cells, could be functionally important” details principal investigator
Next, the Mikkola group teamed up with
The study also revealed that the ring cells exert contractile force through the actomyosin network, via non-muscle myosin IIA (NMIIA). The functionality of ring cells was impaired in NMIIA deficient mice leading to compromised mammary bud shape. Whether other developing organs utilize a similar cellular mechanism for invagination remains an open question.
Original article
Trela E, Lan Q, Myllymäki SM, Villeneuve C, Lindström R, Kumar V, Wickström SA, Mikkola ML.
Further information
- Marja Mikkola,
- Ewelina Trela,