Cargando…

Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland

Actin filament-associated protein 1 (AFAP1) is an adaptor protein of cSrc that binds to filamentous actin and regulates the activity of this tyrosine kinase to affect changes to the organization of the actin cytoskeleton. In breast and prostate cancer cells, AFAP1 has been shown to regulate cellular...

Descripción completa

Detalles Bibliográficos
Autores principales: Cunnick, Jess M, Kim, Stephanie, Hadsell, James, Collins, Stephen, Cerra, Carmine, Reiser, Patti, Flynn, Daniel C, Cho, Youngjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302073/
https://www.ncbi.nlm.nih.gov/pubmed/25043309
http://dx.doi.org/10.1038/onc.2014.205
_version_ 1782353730758246400
author Cunnick, Jess M
Kim, Stephanie
Hadsell, James
Collins, Stephen
Cerra, Carmine
Reiser, Patti
Flynn, Daniel C
Cho, Youngjin
author_facet Cunnick, Jess M
Kim, Stephanie
Hadsell, James
Collins, Stephen
Cerra, Carmine
Reiser, Patti
Flynn, Daniel C
Cho, Youngjin
author_sort Cunnick, Jess M
collection PubMed
description Actin filament-associated protein 1 (AFAP1) is an adaptor protein of cSrc that binds to filamentous actin and regulates the activity of this tyrosine kinase to affect changes to the organization of the actin cytoskeleton. In breast and prostate cancer cells, AFAP1 has been shown to regulate cellular responses requiring actin cytoskeletal changes such as adhesion, invadopodia formation and invasion. However, a normal physiological role for AFAP1 has remained elusive. In this study, we generated an AFAP1 knockout mouse model that establishes a novel physiological role for AFAP1 in lactation. Specifically, these animals displayed a defect in lactation that resulted in an inability to efficiently nurse. Histologically, the mammary glands of the lactating knockout mice were distinguished by the accumulation of large cytoplasmic lipid droplets in the alveolar epithelial cells. There was a reduction in lipid synthesis and the expression of lipogenic genes without a corresponding reduction in the production of beta-casein, a milk protein. Furthermore, these defects were associated with histological and biochemical signs of precocious involution. This study also demonstrated that AFAP1 responds to prolactin, a lactogenic hormone, by forming a complex with cSrc and becoming tyrosine phosphorylated. Together, these observations pointed to a defect in secretory activation. Certain characteristics of this phenotype mirrored the defect in secretory activation in the cSrc knockout mouse, but most importantly, the activity of cSrc in the mammary gland was reduced during early lactation in the AFAP1 null mouse and the localization of active cSrc at the apical surface of luminal epithelial cells during lactation was selectively lost in the absence of AFAP1. These data define, for the first time, the requirement of AFAP1 for the spatial and temporal regulation of cSrc activity in the normal breast, specifically for milk production.
format Online
Article
Text
id pubmed-4302073
institution National Center for Biotechnology Information
language English
publishDate 2014
record_format MEDLINE/PubMed
spelling pubmed-43020732015-11-14 Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland Cunnick, Jess M Kim, Stephanie Hadsell, James Collins, Stephen Cerra, Carmine Reiser, Patti Flynn, Daniel C Cho, Youngjin Oncogene Article Actin filament-associated protein 1 (AFAP1) is an adaptor protein of cSrc that binds to filamentous actin and regulates the activity of this tyrosine kinase to affect changes to the organization of the actin cytoskeleton. In breast and prostate cancer cells, AFAP1 has been shown to regulate cellular responses requiring actin cytoskeletal changes such as adhesion, invadopodia formation and invasion. However, a normal physiological role for AFAP1 has remained elusive. In this study, we generated an AFAP1 knockout mouse model that establishes a novel physiological role for AFAP1 in lactation. Specifically, these animals displayed a defect in lactation that resulted in an inability to efficiently nurse. Histologically, the mammary glands of the lactating knockout mice were distinguished by the accumulation of large cytoplasmic lipid droplets in the alveolar epithelial cells. There was a reduction in lipid synthesis and the expression of lipogenic genes without a corresponding reduction in the production of beta-casein, a milk protein. Furthermore, these defects were associated with histological and biochemical signs of precocious involution. This study also demonstrated that AFAP1 responds to prolactin, a lactogenic hormone, by forming a complex with cSrc and becoming tyrosine phosphorylated. Together, these observations pointed to a defect in secretory activation. Certain characteristics of this phenotype mirrored the defect in secretory activation in the cSrc knockout mouse, but most importantly, the activity of cSrc in the mammary gland was reduced during early lactation in the AFAP1 null mouse and the localization of active cSrc at the apical surface of luminal epithelial cells during lactation was selectively lost in the absence of AFAP1. These data define, for the first time, the requirement of AFAP1 for the spatial and temporal regulation of cSrc activity in the normal breast, specifically for milk production. 2014-07-21 2015-05-14 /pmc/articles/PMC4302073/ /pubmed/25043309 http://dx.doi.org/10.1038/onc.2014.205 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Cunnick, Jess M
Kim, Stephanie
Hadsell, James
Collins, Stephen
Cerra, Carmine
Reiser, Patti
Flynn, Daniel C
Cho, Youngjin
Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title_full Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title_fullStr Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title_full_unstemmed Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title_short Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland
title_sort actin filament-associated protein 1 is required for csrc activity and secretory activation in the lactating mammary gland
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302073/
https://www.ncbi.nlm.nih.gov/pubmed/25043309
http://dx.doi.org/10.1038/onc.2014.205
work_keys_str_mv AT cunnickjessm actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT kimstephanie actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT hadselljames actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT collinsstephen actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT cerracarmine actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT reiserpatti actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT flynndanielc actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland
AT choyoungjin actinfilamentassociatedprotein1isrequiredforcsrcactivityandsecretoryactivationinthelactatingmammarygland