| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-101 |
Sentence |
denotes |
Protein kinase C and calcineurin synergize to activate IkappaB kinase and NF-kappaB in T lymphocytes. |
| T1 |
0-101 |
Sentence |
denotes |
Protein kinase C and calcineurin synergize to activate IkappaB kinase and NF-kappaB in T lymphocytes. |
| T2 |
102-250 |
Sentence |
denotes |
The nuclear factor of kappaB (NF-kappaB) is a ubiquitous transcription factor that is key in the regulation of the immune response and inflammation. |
| T2 |
102-250 |
Sentence |
denotes |
The nuclear factor of kappaB (NF-kappaB) is a ubiquitous transcription factor that is key in the regulation of the immune response and inflammation. |
| T3 |
251-410 |
Sentence |
denotes |
T cell receptor (TCR) cross-linking is in part required for activation of NF-kappaB, which is dependent on the phosphorylation and degradation of IkappaBalpha. |
| T3 |
251-410 |
Sentence |
denotes |
T cell receptor (TCR) cross-linking is in part required for activation of NF-kappaB, which is dependent on the phosphorylation and degradation of IkappaBalpha. |
| T4 |
411-752 |
Sentence |
denotes |
By using Jurkat and primary human T lymphocytes, we demonstrate that the simultaneous activation of two second messengers of the TCR-initiated signal transduction, protein kinase C (PKC) and calcineurin, results in the synergistic activation of the IkappaBalpha kinase (IKK) complex but not of another putative IkappaBalpha kinase, p90(rsk). |
| T4 |
411-752 |
Sentence |
denotes |
By using Jurkat and primary human T lymphocytes, we demonstrate that the simultaneous activation of two second messengers of the TCR-initiated signal transduction, protein kinase C (PKC) and calcineurin, results in the synergistic activation of the IkappaBalpha kinase (IKK) complex but not of another putative IkappaBalpha kinase, p90(rsk). |
| T5 |
753-929 |
Sentence |
denotes |
We also demonstrate that the IKK complex, but not p90(rsk), is responsible for the in vivo phosphorylation of IkappaBalpha mediated by the co-activation of PKC and calcineurin. |
| T5 |
753-929 |
Sentence |
denotes |
We also demonstrate that the IKK complex, but not p90(rsk), is responsible for the in vivo phosphorylation of IkappaBalpha mediated by the co-activation of PKC and calcineurin. |
| T6 |
930-1078 |
Sentence |
denotes |
Each second messenger is necessary, as inhibition of either one reverses the activation of the IKK complex and IkappaBalpha phosphorylation in vivo. |
| T6 |
930-1078 |
Sentence |
denotes |
Each second messenger is necessary, as inhibition of either one reverses the activation of the IKK complex and IkappaBalpha phosphorylation in vivo. |
| T7 |
1079-1212 |
Sentence |
denotes |
Overexpression of dominant negative forms of IKKalpha and -beta demonstrates that only IKKbeta is the target for PKC and calcineurin. |
| T7 |
1079-1212 |
Sentence |
denotes |
Overexpression of dominant negative forms of IKKalpha and -beta demonstrates that only IKKbeta is the target for PKC and calcineurin. |
| T8 |
1213-1405 |
Sentence |
denotes |
These results indicate that within the TCR/CD3 signal transduction pathway both PKC and calcineurin are required for the effective activation of the IKK complex and NF-kappaB in T lymphocytes. |
| T8 |
1213-1405 |
Sentence |
denotes |
These results indicate that within the TCR/CD3 signal transduction pathway both PKC and calcineurin are required for the effective activation of the IKK complex and NF-kappaB in T lymphocytes. |