Stat5 expression is critical for mast cell development and survival

Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects...

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Veröffentlicht in:Blood 2003-08, Vol.102 (4), p.1290-1297
Hauptverfasser: Shelburne, Christopher P., McCoy, Margaret E., Piekorz, Roland, Sexl, Veronica, Roh, Kwan-Ho, Jacobs-Helber, Sarah M., Gillespie, Sheila R., Bailey, Daniel P., Mirmonsef, Paria, Mann, Meredith N., Kashyap, Mohit, Wright, Harry V., Chong, Hey Jin, Bouton, L. Andrew, Barnstein, Brian, Ramirez, Carlos D., Bunting, Kevin D., Sawyer, Steven, Lantz, Chris S., Ryan, John J.
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container_end_page 1297
container_issue 4
container_start_page 1290
container_title Blood
container_volume 102
creator Shelburne, Christopher P.
McCoy, Margaret E.
Piekorz, Roland
Sexl, Veronica
Roh, Kwan-Ho
Jacobs-Helber, Sarah M.
Gillespie, Sheila R.
Bailey, Daniel P.
Mirmonsef, Paria
Mann, Meredith N.
Kashyap, Mohit
Wright, Harry V.
Chong, Hey Jin
Bouton, L. Andrew
Barnstein, Brian
Ramirez, Carlos D.
Bunting, Kevin D.
Sawyer, Steven
Lantz, Chris S.
Ryan, John J.
description Interleukin-3 (IL-3) and stem cell factor (SCF) are important mast cell growth and differentiation factors. Since both cytokines activate the transcription factor signal transducer and activator of transcription 5 (Stat5), a known regulator of proliferation and survival, we investigated the effects of Stat5 deficiency on mast cell development and survival. Bone marrow–derived mast cell (BMMC) populations cultured from Stat5A/B-deficient mice survived in IL-3 + SCF, but not in either cytokine alone. These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. These results indicate that Stat5A and Stat5B are critical regulators of in vitro and in vivo mast cell development and survival.
doi_str_mv 10.1182/blood-2002-11-3490
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Bone marrow–derived mast cell (BMMC) populations cultured from Stat5A/B-deficient mice survived in IL-3 + SCF, but not in either cytokine alone. These cells demonstrated reduced expression of Bcl-2, Bcl-x(L), cyclin A2, and cyclin B1, with increased apoptosis and delayed cell cycle progression during IL-3 or SCF culture. Finally, the absence of Stat5 resulted in loss of in vivo mast cell development, as judged by assessments of Stat5-deficient mice and transplantation of Stat5-deficient bone marrow cells to mast cell-deficient recipient mice. 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subjects Allergic diseases
Animals
Biological and medical sciences
Caspases - metabolism
Cells, Cultured
Cyclins - biosynthesis
Cyclins - genetics
DNA-Binding Proteins - biosynthesis
DNA-Binding Proteins - deficiency
DNA-Binding Proteins - physiology
Enzyme Activation - genetics
General aspects
Humans
Immunopathology
Interleukin-3 - pharmacology
Mast Cells - cytology
Mast Cells - physiology
Medical sciences
Mice
Mice, Inbred C57BL
Milk Proteins
Mitochondria - physiology
Proto-Oncogene Proteins c-bcl-2 - biosynthesis
Recombinant Proteins - pharmacology
Signal Transduction - drug effects
Signal Transduction - physiology
STAT5 Transcription Factor
Stem Cell Factor - pharmacology
Trans-Activators - biosynthesis
Trans-Activators - deficiency
Trans-Activators - physiology
Tumor Suppressor Proteins
Up-Regulation
title Stat5 expression is critical for mast cell development and survival
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