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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=RAB27A</id>
	<title>RAB27A - История изменений</title>
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	<updated>2026-06-22T02:00:31Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=RAB27A&amp;diff=4088&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Ras-related protein Rab-27A (EC 3.6.5.2) (Rab-27) (GTP-binding protein Ram) [RAB27]  ==Publications==  {{medline-entry |title=Reduced expression level of the cycl...»</title>
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		<updated>2021-04-29T18:59:54Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Ras-related protein Rab-27A (EC 3.6.5.2) (Rab-27) (GTP-binding protein Ram) [RAB27]  ==Publications==  {{medline-entry |title=Reduced expression level of the cycl...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Ras-related protein Rab-27A (EC 3.6.5.2) (Rab-27) (GTP-binding protein Ram) [RAB27]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Reduced expression level of the cyclic adenosine monophosphate response element-binding protein contributes to lung aging.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23991634&lt;br /&gt;
|abstract=Lung aging is associated with morphological and physiological changes in which alterations in transcription factors, including the cyclic adenosine monophosphate response element-binding protein (CREB), could play a role. We studied CREB in lung tissue from mice at different ages and in response to known age-related factors (e.g., cellular senescence and matrix modifications with advanced glycation end-products [AGEs]). Our study shows that protein but not mRNA levels of CREB are reduced in the lungs of old mice. CREB reduction was also observed in senescent human lung fibroblasts (WI-38, LuFi) and human lung epithelial cells (A549) cultured on AGE-modified collagen matrix. Reduction of CREB protein is partially based on pre- and posttranslational modifications as exhibited by an increase in the CREB-regulating microRNA 34b and CREB ubiquitination. Permanent down-regulation of CREB in lung cells impaired cell proliferation and viability and increased the number of cells with senescence-associated β-galactosidase activity. CREB down-regulation was accompanied by the reduced expression of 165 genes in WI-38 fibroblasts and A549 epithelial cells, of which 15 genes showed a reduced expression in lung tissues of old mice. The CREB-dependent reduction in [[RAB27A]] coding for the Ras-related protein Rab27A and [[IGFBP3]] coding for the insulin-like growth factor-binding protein 3 has been confirmed for aged lung tissue, senescent fibroblasts, and lung epithelial cells on AGE-modified collagen. Our data demonstrate that the reduced protein expression of CREB might play a significant role in lung aging by modifying the transcription of [[RAB27A]], [[IGFBP3]], and other target genes. &lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Cell Line, Tumor&lt;br /&gt;
* Cell Proliferation&lt;br /&gt;
* Cell Survival&lt;br /&gt;
* Cellular Senescence&lt;br /&gt;
* Cyclic AMP&lt;br /&gt;
* Cyclic AMP Response Element-Binding Protein&lt;br /&gt;
* Down-Regulation&lt;br /&gt;
* Epithelial Cells&lt;br /&gt;
* Fibroblasts&lt;br /&gt;
* Humans&lt;br /&gt;
* Insulin-Like Growth Factor Binding Protein 3&lt;br /&gt;
* Lung&lt;br /&gt;
* Mice&lt;br /&gt;
* Mice, Inbred C57BL&lt;br /&gt;
* MicroRNAs&lt;br /&gt;
* Protein Modification, Translational&lt;br /&gt;
* RNA Processing, Post-Transcriptional&lt;br /&gt;
* Ubiquitination&lt;br /&gt;
* beta-Galactosidase&lt;br /&gt;
* rab GTP-Binding Proteins&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1165/rcmb.2013-0057OC&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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