Mn 2؉ treatment has been shown to promote neurite outgrowth in rat pheochromocytoma (PC12) cells in a time-and dose-dependent manner. This process is mediated through the interactions of extracellular matrix (ECM) proteins and integrin receptors. Studies were performed to determine whether the phosp
P2Y2 receptors induced cell surface redistribution of αv integrin is required for activation of ERK 1/2 in U937 cells
✍ Scribed by Nataliya E. Chorna; Migdalia Chevres; Cynthia Santos-Berrios; Elsie A. Orellano; Laurie Erb; Fernando A. González
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 605 KB
- Volume
- 211
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Nucleotides released from cells due to stress, injury or inflammation, induce mitogenic effects in monocytes via activation of P2Y~2~ nucleotide receptors (P2Y~2~Rs). Here we show that P2Y~2~ nucleotide receptors in U937 monocytic cells regulate the activation of extracellular signal‐regulated kinases 1 and 2 (ERK 1/2) by inducing the clustering of α~v~ integrins. The activation of phosphatidylinositol 3‐kinase by P2Y~2~R ligands was required for α~v~ clustering, suggesting a means whereby two different classes of receptors communicate to induce mitogenic responses in monocytic cells. P2Y~2~R‐induced α~v~ clustering was also associated with a flattened phenotype of the U937 cells, consistent with the role of the P2Y~2~R in regulating early events in cell migration. J. Cell. Physiol. 211: 410–422, 2007. © 2006 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
The mechanism of the induction of apoptosis by arsenic trioxide (As 2 O 3 ), which was demonstrated recently to be an effective inducer of apoptosis in patients with leukemia, was examined in detail in human leukemia U937 cells. Upon treatment of U937 cells with 50 M of As 2 O 3 , complete inactivat
## Abstract The aim of the present study is to explore the signaling pathway associated with __Naja naja atra__ phospholipase A~2~ (PLA~2~)‐induced apoptotic death of human leukemia U937 cells. Degradation of procaspases, production of tBid, loss of mitochondrial membrane potential, and cytochrome