Induction of apoptosis by a secreted lipocalin that is transcriptionally regulated by IL-3 deprivation
Devireddy, Laxminarayana R. ; Teodoro, Jose G. ; Richard, Fabien A. ; Green, Michael R.
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Keywords
Animals
*Apoptosis
Autocrine Communication
Carrier Proteins
Cell Line
Cells, Cultured
Culture Media, Conditioned
Dexamethasone
*Gene Expression Regulation
Humans
Insulin-Like Growth Factor I
Interleukin-3
Interleukins
Leukocytes
Lipocalins
Mice
Oligonucleotide Array Sequence Analysis
Oncogene Proteins
Phosphorylation
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-bcl-2
Receptors, Cell Surface
Recombinant Fusion Proteins
Transcription, Genetic
Tumor Cells, Cultured
bcl-Associated Death Protein
bcl-X Protein
Life Sciences
Medicine and Health Sciences
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Abstract
Many hematopoietic cells undergo apoptosis when deprived of specific cytokines, and this process requires de novo RNA/protein synthesis. Using DNA microarrays to analyze interleukin-3 (IL-3)-dependent murine FL5.12 pro-B cells, we found that the gene undergoing maximal transcriptional induction after cytokine withdrawal is 24p3, which encodes a secreted lipocalin. Conditioned medium from IL-3-deprived FL5.12 cells contained 24p3 and induced apoptosis in naive FL5.12 cells even when IL-3 was present. 24p3 also induced apoptosis in a wide variety of leukocytes but not other cell types. Apoptotic sensitivity correlated with the presence of a putative 24p3 cell surface receptor. We conclude that IL-3 deprivation activates 24p3 transcription, leading to synthesis and secretion of 24p3, which induces apoptosis through an autocrine pathway.
Source
Science. 2001 Aug 3;293(5531):829-34. Link to article on publisher's site