Ceramides signaling pathway
Ceramides regulate diverse signaling pathways involving
apoptosis, cell senescence, the cell cycle, and differentiation.
Preliminary Ceramides effects are antagonistic to growth and
survival [1], [2].
Ceramides levels are elevated in response to diverse stress
challenges including irradiation, heat and cytokines. For instance, Ceramides
act as second messengers in tumor necrosis factor (TNF-alpha)/
Tumor necrosis factor receptor superfamily, member 1 (TNF-R1)
signaling [1], [2],
[3]. TNF-R1 binds adaptor Neutral
sphingomyelinase activation associated factor (FAN) that
transducer signal to Neutral sphingomyelinase [4].
TNF-R1 activates Acid sphingomyelinase via pathway, which
require TNFRSF1A-associated via death domain (TRADD)/ Fas
(TNFRSF6)-associated via death domain (FADD) adaptor proteins [5],
[6]. Acid and Neutral sphingomyelinases
probably can trigger different TNF-alpha-induced pathways. Ceramide
produced by Neutral sphingomyelinase stimulates Ceramides-activated
Mitogen-activated protein kinase 1 and 3 (ERK1/2) cascade and Acid
sphingomyelinase may couple the TNF-R1 to the secretary
pathway and to apoptosis via Cathepsin D [6].
Ceramides induce TNF-alpha/ ERK1/2 cascade via
Kinase suppressor of ras 1 (KSR). KSR is a molecular
scaffold coordinating the Raf (v-myc myelocytomatosis viral oncogene
homolog (c-Raf-1))/ Mitogen-activated protein kinase kinase 1 (MEK1)
interaction [7], [8],
[9]. Ceramides signaling in some cases was
shown to be dependent on v-Ha-ras Harvey rat sarcoma viral oncogene
homolog (H-Ras) [8], [10].
This can be explained by scaffolding properties of KSR [9].
TNF-alpha and Ceramides activation of H-Ras leads
to Phosphoinositide-3-kinase (PI3K reg class IA (p85))/ PI3K
cat) activation and then to fibroblasts proliferation [10].
And controversially, KSR/ c-Raf-1/ MEK1(MAP2K1) [8]/
ERK1/2 [7] -dependent pathway can
lead to inhibition of PI3K/ v-akt murine thymoma viral oncogene
homolog (AKT(PKB)) activation. This prevents BCL2-associated
agonist of cell death (BAD) phosphorylation and leads to
apoptosis in COS-7 cells. The mechanism is not elucidated [7],
[8], [11]. Also,
Inhibition of AKT(PKB) by Ceramides can be a pathway of Ceramides-induced
inhibition of Insulin-induced glucose uptake. Ceramides can
suppress AKT(PKB) activity without PI3K inhibition. This
inhibition depends on protein phosphatase 2 (PP2A)-mediated
dephosphorylation and by blocking AKT(PKB) translocation to
plasma membrane via Protein kinase C zeta (PKC-zeta). Ceramides
can directly bind and activate PKC-zeta and PP2A. [12],
[13], [14], [15].
Ceramides can participate in Fas ligand (FasL(TNFSF6))
signaling leading to apoptosis [16], [17],
[18]. FasL(TNFSF6) binds Fas (FasR(CD95))
that induces Caspase-8-mediated Acid sphingomyelinase [19]
and Caspase-3-mediated Neutral sphingomyelinase activation
[20] and production of Ceramides. Ceramides
then promotes Ras-dependent apoptosis [21].
PKC-zeta directly binds and activates Mitogen-activated protein
kinase kinase kinase 1 (MEKK1(MAP3K1)), Mitogen-activated protein
kinase kinase 4 (MEK4(MAP2K4)), Mitogen-activated protein kinase
8 (JNK1(MAPK8)) [22]. Activation of JNK1(MAPK8)
pathway by TNF-alpha and Ceramides leads to apoptosis [23].
Ceramides-induced mitogen-activated protein kinase kinase kinase
7 (TAK1(MAP3K7)) also participates in this process [11],
[24].
Ceramides via Cathepsin D/ BH3 interacting domain death
agonist (Bid)/ Cytochrome c mediates TNF-alpha
induced apoptosis. Mitochondrial pathway of apoptosis includes
activation of Caspases-3 and Caspases-9 [25],
[26], [27].
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