TY - JOUR
T1 - Molecular complexity of mammary glands development
T2 - a review of lactogenic differentiation in epithelial cells
AU - Jena, Manoj Kumar
AU - Khan, Farheen Badrealam
AU - Ali, Syed Azmal
AU - Abdullah, Abdullah
AU - Sharma, Amarish Kumar
AU - Yadav, Vikas
AU - Kancharla, Sudhakar
AU - Kolli, Prachetha
AU - Mandadapu, Gowtham
AU - Sahoo, Anjan Kumar
AU - Rath, Prasana Kumar
AU - Taneera, Jalal
AU - Kumar, Sudarshan
AU - Mohanty, Ashok Kumar
AU - Goh, Khang Wen
AU - Ming, Long Chiau
AU - Ardianto, Chrismawan
N1 - Publisher Copyright:
© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023
Y1 - 2023
N2 - The mammary gland is a dynamic organ with various physiological processes like cellular proliferation, differentiation, and apoptosis during the pregnancy-lactation-involution cycle. It is essential to understand the molecular changes during the lactogenic differentiation of mammary epithelial cells (MECs, the milk-synthesizing cells). The MECs are organized as luminal milk-secreting cells and basal myoepithelial cells (responsible for milk ejection by contraction) that form the alveoli. The branching morphogenesis and lactogenic differentiation of the MECs prepare the gland for lactation. This process is governed by many molecular mediators including hormones, growth factors, cytokines, miRNAs, regulatory proteins, etc. Interestingly, various signalling pathways guide lactation and understanding these molecular transitions from pregnancy to lactation will help researchers design further research. Manipulation of genes responsible for milk synthesis and secretion will promote augmentation of milk yield in dairy animals. Identifying protein signatures of lactation will help develop strategies for persistent lactation and shortening the dry period in farm animals. The present review article discusses in details the physiological and molecular changes occurring during lactogenic differentiation of MECs and the associated hormones, regulatory proteins, miRNAs, and signalling pathways. An in-depth knowledge of the molecular events will aid in developing engineered cellular models for studies related to mammary gland diseases of humans and animals.
AB - The mammary gland is a dynamic organ with various physiological processes like cellular proliferation, differentiation, and apoptosis during the pregnancy-lactation-involution cycle. It is essential to understand the molecular changes during the lactogenic differentiation of mammary epithelial cells (MECs, the milk-synthesizing cells). The MECs are organized as luminal milk-secreting cells and basal myoepithelial cells (responsible for milk ejection by contraction) that form the alveoli. The branching morphogenesis and lactogenic differentiation of the MECs prepare the gland for lactation. This process is governed by many molecular mediators including hormones, growth factors, cytokines, miRNAs, regulatory proteins, etc. Interestingly, various signalling pathways guide lactation and understanding these molecular transitions from pregnancy to lactation will help researchers design further research. Manipulation of genes responsible for milk synthesis and secretion will promote augmentation of milk yield in dairy animals. Identifying protein signatures of lactation will help develop strategies for persistent lactation and shortening the dry period in farm animals. The present review article discusses in details the physiological and molecular changes occurring during lactogenic differentiation of MECs and the associated hormones, regulatory proteins, miRNAs, and signalling pathways. An in-depth knowledge of the molecular events will aid in developing engineered cellular models for studies related to mammary gland diseases of humans and animals.
KW - hormones
KW - lactation
KW - Lactogenic differentiation
KW - mammary epithelial cells
UR - http://www.scopus.com/inward/record.url?scp=85170484840&partnerID=8YFLogxK
U2 - 10.1080/21691401.2023.2252872
DO - 10.1080/21691401.2023.2252872
M3 - Article
C2 - 37694522
AN - SCOPUS:85170484840
SN - 2169-1401
VL - 51
SP - 491
EP - 508
JO - Artificial Cells, Nanomedicine and Biotechnology
JF - Artificial Cells, Nanomedicine and Biotechnology
IS - 1
ER -