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

被引:12
作者
Cunnick, J. M. [1 ]
Kim, S. [2 ]
Hadsell, J. [3 ]
Collins, S.
Cerra, C. [4 ]
Reiser, P. [4 ]
Flynn, D. C. [5 ]
Cho, Y. [1 ]
机构
[1] Commonwealth Med Coll, Dept Basic Sci, Scranton, PA 18509 USA
[2] Commonwealth Med Coll, Grad Sch Med, Scranton, PA 18509 USA
[3] Fortis Inst Scranton, Scranton, PA USA
[4] Pocono Hlth Syst, Dept Pathol, East Stroudsburg, PA USA
[5] Univ Delaware, Coll Hlth Sci, Newark, DE USA
关键词
SRC FAMILY KINASES; C-SRC; PROLACTIN RECEPTOR; AFAP-110; CANCER; PHOSPHORYLATION; EXPRESSION; INTEGRITY; ABILITY; IDENTIFICATION;
D O I
10.1038/onc.2014.205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 physiologic role for AFAP1 has remained elusive. In this study, we generated an AFAP1 knockout mouse model that establishes a novel physiologic role for AFAP1 in lactation. Specifically, these animals displayed a defect in lactation that resulted in an inability to nurse efficiently. 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 histologic 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. Taken 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.
引用
收藏
页码:2640 / 2649
页数:10
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