| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-100 |
Sentence |
denotes |
Rab35 and its GAP EPI64C in T cells regulate receptor recycling and immunological synapse formation. |
| T1 |
0-100 |
Sentence |
denotes |
Rab35 and its GAP EPI64C in T cells regulate receptor recycling and immunological synapse formation. |
| T2 |
101-313 |
Sentence |
denotes |
Upon antigen recognition, T-cell receptor (TCR/CD3) and other signaling molecules become enriched in a specialized contact site between the T cell and antigen-presenting cell, i.e. the immunological synapse (IS). |
| T2 |
101-313 |
Sentence |
denotes |
Upon antigen recognition, T-cell receptor (TCR/CD3) and other signaling molecules become enriched in a specialized contact site between the T cell and antigen-presenting cell, i.e. the immunological synapse (IS). |
| T3 |
314-462 |
Sentence |
denotes |
Enrichment occurs via mechanisms that include polarized secretion from recycling endosomes, but the Rabs and RabGAPs that regulate this are unknown. |
| T3 |
314-462 |
Sentence |
denotes |
Enrichment occurs via mechanisms that include polarized secretion from recycling endosomes, but the Rabs and RabGAPs that regulate this are unknown. |
| T4 |
463-657 |
Sentence |
denotes |
EPI64C (TBC1D10C) is an uncharacterized candidate RabGAP we identified by mass spectrometry as abundant in human peripheral blood T cells that is preferentially expressed in hematopoietic cells. |
| T4 |
463-657 |
Sentence |
denotes |
EPI64C (TBC1D10C) is an uncharacterized candidate RabGAP we identified by mass spectrometry as abundant in human peripheral blood T cells that is preferentially expressed in hematopoietic cells. |
| T5 |
658-767 |
Sentence |
denotes |
EPI64C is a Rab35-GAP based both on in vitro Rab35-specific GAP activity and findings in transfection assays. |
| T5 |
658-767 |
Sentence |
denotes |
EPI64C is a Rab35-GAP based both on in vitro Rab35-specific GAP activity and findings in transfection assays. |
| T6 |
768-1008 |
Sentence |
denotes |
EPI64C and Rab35 dominant negative (DN) constructs each impaired transferrin export from a recycling pathway in Jurkat T-cells and induced large vacuoles marked by transferrin receptor, TCR, and SNAREs implicated in TCR-polarized secretion. |
| T6 |
768-1008 |
Sentence |
denotes |
EPI64C and Rab35 dominant negative (DN) constructs each impaired transferrin export from a recycling pathway in Jurkat T-cells and induced large vacuoles marked by transferrin receptor, TCR, and SNAREs implicated in TCR-polarized secretion. |
| T7 |
1009-1135 |
Sentence |
denotes |
Rab35 localized to the plasma membrane and to intracellular vesicles where it substantially colocalized with TfR and with TCR. |
| T7 |
1009-1135 |
Sentence |
denotes |
Rab35 localized to the plasma membrane and to intracellular vesicles where it substantially colocalized with TfR and with TCR. |
| T8 |
1136-1175 |
Sentence |
denotes |
Rab35 was strongly recruited to the IS. |
| T8 |
1136-1175 |
Sentence |
denotes |
Rab35 was strongly recruited to the IS. |
| T9 |
1176-1274 |
Sentence |
denotes |
Conjugate formation was impaired by transfection with Rab35-DN or EPI64C and by EPI64C knock down. |
| T9 |
1176-1274 |
Sentence |
denotes |
Conjugate formation was impaired by transfection with Rab35-DN or EPI64C and by EPI64C knock down. |
| T10 |
1275-1325 |
Sentence |
denotes |
TCR enrichment at the IS was impaired by Rab35-DN. |
| T10 |
1275-1325 |
Sentence |
denotes |
TCR enrichment at the IS was impaired by Rab35-DN. |
| T11 |
1326-1477 |
Sentence |
denotes |
Thus, EPI64C and Rab35 regulate a recycling pathway in T cells and contribute to IS formation, most likely by participating in TCR transport to the IS. |
| T11 |
1326-1477 |
Sentence |
denotes |
Thus, EPI64C and Rab35 regulate a recycling pathway in T cells and contribute to IS formation, most likely by participating in TCR transport to the IS. |