Related Experiment Video
Updated: Aug 12, 2026

Indirect Immunofluorescence on Frozen Sections of Mouse Mammary Gland
Published on: December 1, 2015
The role of Stat3 in apoptosis and mammary gland involution. Conditional deletion of Stat3
R S Chapman1, P Lourenco, E Tonner
1Dept. of Pathology, University of Edinburgh, UK.
Abstract:
STATs (signal transducer and activator of transcription) are a family of latent transcription factors which are activated in response to a variety of cytokines and growth factors. This family of signalling molecules have been implicated in growth, differentiation, survival and apoptosis. In this article, we will review work which highlights the role of individual STAT factors in mammary gland and demonstrate the value of genetically modified mice in defining the function of STAT3. Involution of the mouse mammary gland is characterised by extensive apoptosis of the epithelial cells and the activation of STAT3. STATs 3 and 5 have reciprocal patterns of activation throughout a mammary developmental cycle suggesting that STAT5 may be a survival factor and STAT3 a death factor for differentiated mammary epithelium. To clarify the role of STAT3 in mammary epithelial apoptosis, we have generated a conditional knockout using the lox/Cre recombination system. Mammary glands from crosses of transgenic mice expressing Cre recombinase under the control of the beta-lactoglobulin milk protein gene promoter with mice harbouring one floxed STAT3 allele and one null STAT3 allele, showed a decrease in epithelial apoptosis and a dramatic delay of the involution process upon forced weaning. This was accompanied by precocious activation of STAT1 and increases in p53 and p21 levels--these may act as a compensatory mechanism for initiating the eventual involution which occurs in STAT3 null mammary glands. This demonstrates for the first time the importance of STAT factors in signalling the initiation of physiological apoptosis in vivo and highlights the utility of the lox/Cre system for addressing the function of genes, which have an embryonic lethal phenotype, specifically in mammary gland.
Insights
Signal transducer and activator of transcription 3 (STAT3) is crucial for mammary gland involution. Conditional knockout of STAT3 in mice delays apoptosis and involution, highlighting STAT factors in initiating physiological apoptosis.
Area of Science:
- Cellular signaling
- Molecular biology
- Developmental biology
Background:
- Signal transducers and Activators of Transcription (STATs) are key transcription factors activated by cytokines and growth factors.
- STATs regulate critical cellular processes including growth, differentiation, survival, and apoptosis.
- STAT3 activation is observed during mouse mammary gland involution, a process marked by epithelial cell apoptosis.
Purpose of the Study:
- To investigate the specific role of STAT3 in mammary epithelial apoptosis during involution.
- To demonstrate the utility of genetically modified mouse models for studying STAT gene function in vivo.
- To elucidate the function of STAT3 in the physiological process of mammary gland involution.
Main Methods:
- Utilized a conditional knockout approach employing the lox/Cre recombination system.
- Generated transgenic mice expressing Cre recombinase under the beta-lactoglobulin promoter.
- Crossed these mice with mice carrying a floxed STAT3 allele and a null STAT3 allele to create mammary gland-specific STAT3 knockouts.
Main Results:
- Mammary glands with conditional STAT3 knockout exhibited reduced epithelial apoptosis.
- Forced weaning led to a significant delay in the involution process in these STAT3-deficient glands.
- Observed precocious activation of STAT1 and increased p53 and p21 levels, suggesting compensatory mechanisms.
Conclusions:
- STAT3 plays a critical role in initiating physiological apoptosis during mammary gland involution.
- The lox/Cre system is effective for studying genes with embryonic lethal phenotypes in specific tissues like the mammary gland.
- STAT factors are essential regulators of mammary gland involution and apoptosis.
Related Concept Videos
Abnormal Proliferation
The JAK-STAT Signaling Pathway
PI3K/mTOR/AKT Signaling Pathway

