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Journal ArticleDOI

Glucocorticoids Stimulate Ribonucleic Acid Degradation in Isolated Rat Thymic Lymphocytes in Vitro

John A. Cidlowski
- 01 Jul 1982 - 
- Vol. 111, Iss: 1, pp 184-190
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TLDR
This data indicates that lymphocytes, which die in response to glucocorticoid, exhibit enhanced rates of cellular protein degradation, which encouraged this work to study the turnover of other lymphocyte cellular macromolecules, namely RNA, as regulated by adrenal steroids.
Abstract
Glucocorticoids are known to stimulate lymphoid cell death, but little information is available regarding the biochemical mechanisms of adrenal steroid-induced lymphocytolysis. Previous work from our laboratory indicates that lymphocytes, which die in response to glucocorticoid, exhibit enhanced rates of cellular protein degradation. These findings encouraged us to study the turnover of other lymphocyte cellular macromolecules, namely RNA, as regulated by adrenal steroids. Thymic lymphocytes were pulse labeled in vitro in Eagle's Minimum Essential Medium supplemented with 10 μCi/ml [3H] uridine. Precursor incorporation into RNA was effectively stopped by a chase/dilution (1:20) of cells into fresh medium supplemented with 10 mM of both unlabeled uridine and cytidine. Cells were incubated in this medium for up to 4 h at 37 C with or without dexamethasone (Dex), and the remaining RNA-associated radioactivity was measured either by acid precipitation or with a multiple automated sample harvester. Control cel...

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Apoptosis: the biochemistry and molecular biology of programmed cell death.

TL;DR: This review first briefly covers some historical perspective on the discovery of apoptotic cell death, the characteristic morphology that accompanies this process, and the numerous cell types and mediators with which programmed cell death is associated.
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Bax Deletion Further Orders the Cell Death Pathway in Cerebellar Granule Cells and Suggests a Caspase-independent Pathway to Cell Death

TL;DR: The results indicate that BAX is required for apoptotic, but not excitotoxic, cell death, and place BAX downstream of metabolic changes, changes in mRNA levels, and increased phosphorylation of c-Jun, yet upstream of the activation of caspases and suggest a caspase-independent death pathway downstream of BAX in cerebellar granule cells.
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Identification of mRNAs associated with programmed cell death in immature thymocytes.

TL;DR: RP-2 and RP-8 are death-associated mRNAs that should be functionally evaluated in the context of the death process, and sequence analysis of RP-2 cDNA indicates the presence of a zinc finger domain suggestive of a possible DNA regulatory role for theRP-8 protein.
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