Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-127 |
Sentence |
denotes |
Human placenta-derived stromal cells decrease inflammation, placental injury, and blood pressure in hypertensive pregnant mice. |
T1 |
0-127 |
Sentence |
denotes |
Human placenta-derived stromal cells decrease inflammation, placental injury, and blood pressure in hypertensive pregnant mice. |
TextSentencer_T2 |
128-382 |
Sentence |
denotes |
Preeclampsia, the development of hypertension and proteinuria or end-organ damage during pregnancy, is a leading cause of both maternal and fetal morbidity and mortality and there are no effective clinical treatments for preeclampsia aside from delivery. |
T2 |
128-382 |
Sentence |
denotes |
Preeclampsia, the development of hypertension and proteinuria or end-organ damage during pregnancy, is a leading cause of both maternal and fetal morbidity and mortality and there are no effective clinical treatments for preeclampsia aside from delivery. |
TextSentencer_T3 |
383-532 |
Sentence |
denotes |
The development of preeclampsia is characterized by maladaptation of the maternal immune system, excessive inflammation, and endothelial dysfunction. |
T3 |
383-532 |
Sentence |
denotes |
The development of preeclampsia is characterized by maladaptation of the maternal immune system, excessive inflammation, and endothelial dysfunction. |
TextSentencer_T4 |
533-703 |
Sentence |
denotes |
We have reported that detection of extracellular RNA by Toll-like receptors (TLRs) 3 and 7 is a key initiating signal that contributes to the development of preeclampsia. |
T4 |
533-703 |
Sentence |
denotes |
We have reported that detection of extracellular RNA by Toll-like receptors (TLRs) 3 and 7 is a key initiating signal that contributes to the development of preeclampsia. |
TextSentencer_T5 |
704-1036 |
Sentence |
denotes |
PLacental eXpanded (PLX-PAD; Pluristem Therapeutics, Inc., Haifa, Israel) cells are human placenta-derived, mesenchymal-like adherent stromal cells that have anti-inflammatory, pro-angiogenic, cytoprotective, and regenerative properties secondary to paracrine secretion of various molecules in response to environmental stimulation. |
T5 |
704-1036 |
Sentence |
denotes |
PLacental eXpanded (PLX-PAD; Pluristem Therapeutics, Inc., Haifa, Israel) cells are human placenta-derived, mesenchymal-like adherent stromal cells that have anti-inflammatory, pro-angiogenic, cytoprotective, and regenerative properties secondary to paracrine secretion of various molecules in response to environmental stimulation. |
TextSentencer_T6 |
1037-1217 |
Sentence |
denotes |
We hypothesized that PLX-PAD cells would reduce the associated inflammation and tissue damage and lower blood pressure in mice with preeclampsia induced by TLR3 or TLR7 activation. |
T6 |
1037-1217 |
Sentence |
denotes |
We hypothesized that PLX-PAD cells would reduce the associated inflammation and tissue damage and lower blood pressure in mice with preeclampsia induced by TLR3 or TLR7 activation. |
TextSentencer_T7 |
1218-1382 |
Sentence |
denotes |
Injection of PLX-PAD cells on gestational day 14 significantly decreased systolic blood pressure by day 17 in TLR3-induced and TLR7-induced hypertensive mice (TLR3: |
T7 |
1218-1382 |
Sentence |
denotes |
Injection of PLX-PAD cells on gestational day 14 significantly decreased systolic blood pressure by day 17 in TLR3-induced and TLR7-induced hypertensive mice (TLR3: |
TextSentencer_T8 |
1383-1408 |
Sentence |
denotes |
144 to 111 mmHg and TLR7: |
T8 |
1383-1408 |
Sentence |
denotes |
144 to 111 mmHg and TLR7: |
TextSentencer_T9 |
1409-1515 |
Sentence |
denotes |
145 to 106 mmHg; both p<0.05), and also normalized their elevated urinary protein/creatinine ratios (TLR3: |
T9 |
1409-1515 |
Sentence |
denotes |
145 to 106 mmHg; both p<0.05), and also normalized their elevated urinary protein/creatinine ratios (TLR3: |
TextSentencer_T10 |
1516-1538 |
Sentence |
denotes |
5.68 to 3.72 and TLR7: |
T10 |
1516-1538 |
Sentence |
denotes |
5.68 to 3.72 and TLR7: |
TextSentencer_T11 |
1539-1566 |
Sentence |
denotes |
5.57 to 3.84; both p<0.05). |
T11 |
1539-1566 |
Sentence |
denotes |
5.57 to 3.84; both p<0.05). |
TextSentencer_T12 |
1567-1765 |
Sentence |
denotes |
Gestational day 17 aortic endothelium-dependent relaxation responses improved significantly in TLR3-induced and TLR7-induced hypertensive mice who received PLX-PAD cells on gestational day 14 (TLR3: |
T12 |
1567-1765 |
Sentence |
denotes |
Gestational day 17 aortic endothelium-dependent relaxation responses improved significantly in TLR3-induced and TLR7-induced hypertensive mice who received PLX-PAD cells on gestational day 14 (TLR3: |
TextSentencer_T13 |
1766-1785 |
Sentence |
denotes |
35 to 65% and TLR7: |
T13 |
1766-1785 |
Sentence |
denotes |
35 to 65% and TLR7: |
TextSentencer_T14 |
1786-1810 |
Sentence |
denotes |
37 to 63%; both p<0.05). |
T14 |
1786-1810 |
Sentence |
denotes |
37 to 63%; both p<0.05). |
TextSentencer_T15 |
1811-1978 |
Sentence |
denotes |
Additionally, markers of systemic inflammation and placental injury, increased markedly in both groups of TLR-induced hypertensive mice, were reduced by PLX-PAD cells. |
T15 |
1811-1978 |
Sentence |
denotes |
Additionally, markers of systemic inflammation and placental injury, increased markedly in both groups of TLR-induced hypertensive mice, were reduced by PLX-PAD cells. |
TextSentencer_T16 |
1979-2089 |
Sentence |
denotes |
Importantly, PLX-PAD cell therapy had no effects on these measures in pregnant control mice or on the fetuses. |
T16 |
1979-2089 |
Sentence |
denotes |
Importantly, PLX-PAD cell therapy had no effects on these measures in pregnant control mice or on the fetuses. |
TextSentencer_T17 |
2090-2266 |
Sentence |
denotes |
These data demonstrate that PLX-PAD cell therapy can safely reverse preeclampsia-like features during pregnancy and have a potential therapeutic role in preeclampsia treatment. |
T17 |
2090-2266 |
Sentence |
denotes |
These data demonstrate that PLX-PAD cell therapy can safely reverse preeclampsia-like features during pregnancy and have a potential therapeutic role in preeclampsia treatment. |