Human placenta-derived stromal cells decrease inflammation, placental injury and blood pressure in hypertensive pregnant mice

被引:27
作者
Chatterjee, Piyali [1 ]
Chiasson, Valorie L. [1 ]
Pinzur, Lena [2 ]
Raveh, Shani [2 ]
Abraham, Eytan [2 ]
Jones, Kathleen A. [3 ]
Bounds, Kelsey R. [1 ]
Ofir, Racheli [2 ]
Flaishon, Liat [2 ]
Chajut, Ayelet [2 ]
Mitchell, Brett M. [1 ]
机构
[1] Baylor Scott & White Hlth, Texas A&M Hlth Sci Ctr, Div Nephrol & Hypertens, Dept Internal Med, 702 SW HK Dodgen Loop, Temple, TX USA
[2] Pluristem Therapeut Inc, IL-31905 Haifa, Israel
[3] Baylor Scott & White Hlth, Texas A&M Hlth Sci Ctr, Dept Pathol, Temple, TX USA
关键词
hypertension; immunity; pre-eclampsia; Toll-like receptors; vascular diseases; ISCHEMIC-HEART-DISEASE; VASCULAR-DYSFUNCTION; IN-VIVO; PREECLAMPSIA; INTERLEUKIN-15; EXPRESSION; COHORT; WOMEN; MODEL; RISK;
D O I
10.1042/CS20150555
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pre-eclampsia, 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 pre-eclampsia aside from delivery. The development of pre-eclampsia is characterized by maladaptation of the maternal immune system, excessive inflammation and endothelial dysfunction. We have reported that detection of extracellular RNA by the Toll-like receptors (TLRs) 3 and 7 is a key initiating signal that contributes to the development of pre-eclampsia. PLacental eXpanded (PLX-PAD) cells are human placenta-derived, mesenchymal-like, adherent stromal cells that have anti-inflammatory, proangiogenic, cytoprotective and regenerative properties, secondary to paracrine secretion of various molecules in response to environmental stimulation. We hypothesized that PLX-PAD cells would reduce the associated inflammation and tissue damage and lower blood pressure in mice with pre-eclampsia induced by TLR3 or TLR7 activation. 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 144-111 mmHg; TLR7 145-106 mmHg; both P<0.05), and also normalized their elevated urinary protein: creatinine ratios (TLR3 5.68-3.72; TLR7 5.57-3.84; both P<0.05). On gestational day 17, aortic endothelium-dependent relaxation responses improved significantly in TLR3-induced and TLR7-induced hypertensive mice that received PLX-PAD cells on gestational day 14 (TLR3 35-65 %; TLR7 37-63 %; both P<0.05). In addition, markers of systemic inflammation and placental injury, increased markedly in both groups of TLR-induced hypertensive mice, were reduced by PLX-PAD cells. Importantly, PLX-PAD cell therapy had no effects on these measures in pregnant control mice or on the fetuses. These data demonstrate that PLX-PAD cell therapy can safely reverse pre-eclampsia-like features during pregnancy and have a potential therapeutic role in pre-eclampsia treatment.
引用
收藏
页码:513 / 523
页数:11
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