Hormone-responsive progenitors have a unique identity and exhibit high motility during mammary morphogenesis

Hormone-receptor-positive (HR<sup>+</sup>) luminal cells largely mediate the response to estrogen and progesterone during mammary gland morphogenesis. However, there remains a lack of consensus on the precise nature of the precursor cells that maintain this essential HR<sup>+</sup> lineage. Here we refine the identification of HR<sup>+</sup> progenitors and demonstrate their unique regenerative capacity compared to mature HR<sup>+</sup> cells. HR<sup>+</sup> progenitors proliferate but do not expand, suggesting rapid differentiation. Subcellular resolution, 3D intravital microscopy was performed on terminal end buds (TEBs) during puberty to dissect the contribution of each luminal lineage. Surprisingly, HR<sup>+</sup> TEB progenitors were highly elongated and motile compared to columnar HR<sup>-</sup> progenitors and static, conoid HR<sup>+</sup> cells within ducts. This dynamic behavior was also observed in response to hormones. Development of an AI model for motility dynamics analysis highlighted stark behavioral changes in HR<sup>+</sup> progenitors as they transitioned to mature cells. This work provides valuable insights into how progenitor behavior contributes to mammary morphogenesis.

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Publication Details

Journal
Cell Reports
Published
2024-12-01
DOI
https://doi.org/10.1016/j.celrep.2024.115073
Citations
8
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
2.26

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article

Hormone-responsive progenitors have a unique identity and exhibit high motility during mammary morphogenesis

Felicity C. Jackling, Bianca D. Capaldo, François Vaillant, Jane E. Visvader et al.
8 citations
Cell Reports
Cancer Cells and Metastasis
2.26
article

Hormone-responsive progenitors have a unique identity and exhibit high motility during mammary morphogenesis

Felicity C. Jackling, Bianca D. Capaldo, François Vaillant, Jane E. Visvader, Caleb A. Dawson, Xiaoyu Song, Lexie Prokopuk, Gordon K. Smyth, Yunshun Chen, Raymond K. H. Yip, Michael J. G. Milevskiy, Geoffrey J. Lindeman
article en
8 citations

Abstract

Hormone-receptor-positive (HR<sup>+</sup>) luminal cells largely mediate the response to estrogen and progesterone during mammary gland morphogenesis. However, there remains a lack of consensus on the precise nature of the precursor cells that maintain this essential HR<sup>+</sup> lineage. Here we refine the identification of HR<sup>+</sup> progenitors and demonstrate their unique regenerative capacity compared to mature HR<sup>+</sup> cells. HR<sup>+</sup> progenitors proliferate but do not expand, suggesting rapid differentiation. Subcellular resolution, 3D intravital microscopy was performed on terminal end buds (TEBs) during puberty to dissect the contribution of each luminal lineage. Surprisingly, HR<sup>+</sup> TEB progenitors were highly elongated and motile compared to columnar HR<sup>-</sup> progenitors and static, conoid HR<sup>+</sup> cells within ducts. This dynamic behavior was also observed in response to hormones. Development of an AI model for motility dynamics analysis highlighted stark behavioral changes in HR<sup>+</sup> progenitors as they transitioned to mature cells. This work provides valuable insights into how progenitor behavior contributes to mammary morphogenesis.

Cell ReportsVol. 43(12)
The Royal Melbourne Hospital (AU), Walter and Eliza Hall Institute of Medical Research (AU)
Breast Cancer Research Foundation, Medical Research Council, National Health and Medical Research Council
Zero hunger
Openalex Percentile: Top 9%
Cancer Cells and Metastasis
2.26
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