Some protein kinases operate in more than one mitogen-activated protein-kinase (MAPK) cascade. We here address the question whether specificity of the cascades necessitates physical sequestration of these "promiscuous" kinases (e.g. by binding to scaffolds). A model is constructed, in which two MAPK
MAP kinase cascade in astrocytes
โ Scribed by Cathy Tournier; Martine Pomerance; Jean Michel Gavaret; Michel Pierre
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 790 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
โฆ Synopsis
We have studied in cultured rat astroglial cells MAP kinases, known for their role in intracellular signal transduction. The MAP kinase activity was stimulated by growth factors (FGFb, FGFa, EGF, PDGF, and IGFl), by a phorbol ester (TPA) activating-protein kinase C (PKC), by a neuropeptide (endothelin-l), and by a neuromediator (carbachol). Astrocytes pretreated for 18 h with TPA were still stimulated by growth factors and endothelin, suggesting that down-regulated isoforms of PKC are not involved in MAP kinase activation. In contrast, the small effect of carbachol was suppressed by TPA pretreatment. Astrocytes contained two proteins (p41 and p44) recognized by MAP kinase antibody. These proteins were phosphorylated on tyrosine residues in the cytosols of stimulated astrocytes.
The kinetics of MAP kinase activation by FGFb and IGFl were very different. FGFb promoted a rapid activation of MAP kinase (about 10 min) plus a prolonged phase that lasted at least 12 h. IGFl produced only a rapid transient peak of activation at about 20 min. Hence, extracellular signals might generate different effects in astrocytes by differentially modulating the MAP kinase cascade.
On a Mono Q column the growth factor-stimulated MAP kinase activity was separated into two peaks containing p41 and p44. Stimulation of astrocytes altered the elution pattern of p44 as a result of its phosphorylation. An ATP-dependent MAP kinase activator (MW = 40-45 kDa) was found in fractions of FGFb-stimulated cells which were not retained on Mono Q column, indicating the existence of a MAP kinase kinase (MEK) in astrocytes. C-Raf, identified in other cells as a MAP kinase kinase kinase, was also present in astrocytes.
Thus astrocytes contain many components of the MAP kinase cascade activated by growth factors that may also be implicated in the action of neuropeptides and neuromediators. o 1994 Wiley-Liss, Inc.
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