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. Author manuscript; available in PMC: 2013 Mar 24.
Published in final edited form as: Physiology (Bethesda). 2011 Apr;26(2):83–96. doi: 10.1152/physiol.00044.2010

Table 2.

Effect ofSepsis/LPS on signaling to and from mTOR substrates and regulatory proteins

Protein Modification Direction/Magnitude Citation
Rat pAkt T308, S473 Decreased 50% (14, 32, 50)
Mouse pAkt S473 No Change (62)
pPRAS40 T246 Decreased 50% (32, 50)
pmTOR S2448/S2481 Decreased 20–50% (50, 54, 59)
pTSC2 S939, T1462 No Change (32, 50)
TSC1/2 Association No Change (32, 50)
pRaptor pS792 Increased 80% (32, 50)
pAMPKα T172 Increased 50% (50)
Raptor/mTOR Association No Change (50)
Raptor/eIF3b Association Decreased 50% (50, 64)
pS6K1 T389 Decreased Basal 70% (32, 54)
pS6K1 T389 Decreased Leu stimulation 70% (59, 60)
Raptor/S6K1 Association Increased 60% (50)
pS6 S240/S244
S235/S236
Decreased basal, Leu, and IGF-I stimulation 75% (32, 60)
p4E-BP1 T37/T46 Decreased basal and Leu stimulation 80% (33, 54, 59, 60)
4E-BP1/4E Association Increased 50% (54, 59, 60)
4E-BP1/4E Leu induced Disassociation Blocked Completely (59, 60)
Mouse 4E-BP1/Raptor Association Decreased 60% (64)
Rat 4E-BP1/Raptor Association Increased 50% (50)
Deptor Total Protein/Mouse C2C12 Decreased 30% (33)
Deptor Total Protein/Rat Muscle Increased 60% (50)

Observations made in the above table summarize representative data specifically pertaining to skeletal muscleand in some cases C2C12 myotubes. A more in depth analysis may be found in the cited references.