scholarly journals The Interleukin-10 Signal Transduction Pathway and Regulation of Gene Expression in Mononuclear Phagocytes

1999 ◽  
Vol 19 (6) ◽  
pp. 563-573 ◽  
Author(s):  
Raymond P. Donnelly ◽  
Harold Dickensheets ◽  
David S. Finbloom
1998 ◽  
Vol 851 (1 STRESS OF LIF) ◽  
pp. 129-138 ◽  
Author(s):  
DIPAK K. DAS ◽  
NILANJANA MAULIK ◽  
RICHARD M. ENGELMAN ◽  
JOHN A. ROUSOU ◽  
DAVID DEATON ◽  
...  

Platelets ◽  
2020 ◽  
Author(s):  
Sonia Águila ◽  
Ernesto Cuenca-Zamora ◽  
Constantino Martínez ◽  
Raúl Teruel-Montoya

In this chapter, we discuss different topics always using the microRNA as the guiding thread of the review. MicroRNAs, member of small noncoding RNAs family, are an important element involved in gene expression. We cover different issues such as their importance in the differentiation and maturation of megakaryocytes (megakaryopoiesis), as well as the role in platelets formation (thrombopoiesis) focusing on the described relationship between miRNA and critical myeloid lineage transcription factors such as RUNX1, chemokines receptors as CRCX4, or central hormones in platelet homeostasis like TPO, as well as its receptor (MPL) and the TPO signal transduction pathway, that is JAK/STAT. In addition to platelet biogenesis, we review the microRNA participation in platelets physiology and function. This review also introduces the use of miRNAs as biomarkers of platelet function since the detection of pathogenic situations or response to therapy using these noncoding RNAs is getting increasing interest in disease management. Finally, this chapter describes the participation of platelets in cellular interplay, since extracellular vesicles have been demonstrated to have the ability to deliver microRNAs to others cells, modulating their function through intercellular communication, redefining the extracellular vesicles from the so-called “platelet dust” to become mediators of intercellular communication.


2003 ◽  
Vol 2 (5) ◽  
pp. 995-1002 ◽  
Author(s):  
Jeanette M. Quinn ◽  
Janette Kropat ◽  
Sabeeha Merchant

ABSTRACT The Cpx1 and Cyc6 genes of Chlamydomonas reinhardtii are activated in copper-deficient cells via a signal transduction pathway that requires copper response elements (CuREs) and a copper response regulator defined by the CRR1 locus. The two genes can also be activated by provision of nickel or cobalt ions in the medium. The response to nickel ions requires at least one CuRE and also CRR1 function, suggesting that nickel interferes with a component in the nutritional copper signal transduction pathway. Nickel does not act by preventing copper uptake/utilization because (i) holoplastocyanin formation is unaffected in Ni2+-treated cells and (ii) provision of excess copper cannot reverse the Ni-dependent activation of the target genes. The CuRE is sufficient for conferring Ni-responsive expression to a reporter gene, which suggests that the system has practical application as a vehicle for inducible gene expression. The inducer can be removed either by replacing the medium or by chelating the inducer with excess EDTA, either of which treatments reverses the activation of the target genes.


Sign in / Sign up

Export Citation Format

Share Document