Literature DB >> 23810554

Aurora A kinase regulates mammary epithelial cell fate by determining mitotic spindle orientation in a Notch-dependent manner.

Joseph L Regan1, Tony Sourisseau, Kelly Soady, Howard Kendrick, Afshan McCarthy, Chan Tang, Keith Brennan, Spiros Linardopoulos, Donald E White, Matthew J Smalley.   

Abstract

Cell fate determination in the progeny of mammary epithelial stem/progenitor cells remains poorly understood. Here, we have examined the role of the mitotic kinase Aurora A (AURKA) in regulating the balance between basal and luminal mammary lineages. We find that AURKA is highly expressed in basal stem cells and, to a lesser extent, in luminal progenitors. Wild-type AURKA expression promoted luminal cell fate, but expression of an S155R mutant reduced proliferation, promoted basal fate, and inhibited serial transplantation. The mechanism involved regulation of mitotic spindle orientation by AURKA and the positioning of daughter cells after division. Remarkably, this was NOTCH dependent, as NOTCH inhibitor blocked the effect of wild-type AURKA expression on spindle orientation and instead mimicked the effect of the S155R mutant. These findings directly link AURKA, NOTCH signaling, and mitotic spindle orientation and suggest a mechanism for regulating the balance between luminal and basal lineages in the mammary gland.
Copyright © 2013 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23810554     DOI: 10.1016/j.celrep.2013.05.044

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  36 in total

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5.  Expansion of stem cells counteracts age-related mammary regression in compound Timp1/Timp3 null mice.

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Review 6.  The mammary stem cell hierarchy: a looking glass into heterogeneous breast cancer landscapes.

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Review 8.  Connections between cadherin-catenin proteins, spindle misorientation, and cancer.

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Journal:  Tissue Barriers       Date:  2015-05-11

9.  Mammary Stem Cell Self-Renewal Is Regulated by Slit2/Robo1 Signaling through SNAI1 and mINSC.

Authors:  Mimmi S Ballard; Anna Zhu; Naomi Iwai; Michael Stensrud; Aurelia Mapps; Maira Pia Postiglione; Juergen A Knoblich; Lindsay Hinck
Journal:  Cell Rep       Date:  2015-10-01       Impact factor: 9.423

10.  WNT-Mediated Regulation of FOXO1 Constitutes a Critical Axis Maintaining Pubertal Mammary Stem Cell Homeostasis.

Authors:  Amulya Sreekumar; Michael J Toneff; Eajer Toh; Kevin Roarty; Chad J Creighton; George K Belka; Dong-Kee Lee; Jianming Xu; Lewis A Chodosh; JoAnne S Richards; Jeffrey M Rosen
Journal:  Dev Cell       Date:  2017-11-02       Impact factor: 12.270

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