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
相关论文
共 40 条
[1]   A role for TLRs in the regulation of immune cell migration by first trimester trophoblast cells [J].
Abrahams, VM ;
Visintin, I ;
Aldo, PB ;
Guller, S ;
Romero, R ;
Mor, G .
JOURNAL OF IMMUNOLOGY, 2005, 175 (12) :8096-8104
[2]   Expression profiles of interleukin-15 in early and late gestational human placenta and in pre-eclamptic placenta [J].
Agarwal, R ;
Loganath, A ;
Roy, AC ;
Wong, YC ;
Ng, SC .
MOLECULAR HUMAN REPRODUCTION, 2001, 7 (01) :97-101
[3]   Interleukin-15 promotes angiogenesis in vivo [J].
Angiolillo, AL ;
Kanegane, H ;
Sgadari, C ;
Reaman, GH ;
Tosato, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 233 (01) :231-237
[4]   Reduced expression of the epidermal growth factor signaling system in preeclampsia [J].
Armant, D. R. ;
Fritz, R. ;
Kilburn, B. A. ;
Kim, Y. M. ;
Nien, J. K. ;
Maihle, N. J. ;
Romero, R. ;
Leach, R. E. .
PLACENTA, 2015, 36 (03) :270-278
[5]   The uterine NK cell population requires IL-15 but these cells are not required for pregnancy nor the resolution of a Listeria monocytogenes infection [J].
Barber, EM ;
Pollard, JW .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :37-46
[6]   An unexpected tail of VEGF and PlGF in pre-eclampsia [J].
Bates, David O. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2011, 39 :1576-1582
[7]   Preeclampsia: a view through the danger model [J].
Bonney, Elizabeth A. .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2007, 76 (1-2) :68-74
[8]  
Bounds Kelsey R, 2015, Front Cardiovasc Med, V2, P20, DOI 10.3389/fcvm.2015.00020
[9]   Interleukin-15 protects from lethal apoptosis in vivo [J].
BulfonePaus, S ;
Ungureanu, D ;
Pohl, T ;
Lindner, G ;
Paus, R ;
Ruckert, R ;
Krause, H ;
Kunzendorf, U .
NATURE MEDICINE, 1997, 3 (10) :1124-1128
[10]   Placental Toll-Like Receptor 3 and Toll-Like Receptor 7/8 Activation Contributes to Preeclampsia in Humans and Mice [J].
Chatterjee, Piyali ;
Weaver, Laura E. ;
Doersch, Karen M. ;
Kopriva, Shelley E. ;
Chiasson, Valorie L. ;
Allen, Samantha J. ;
Narayanan, Ajay M. ;
Young, Kristina J. ;
Jones, Kathleen A. ;
Kuehl, Thomas J. ;
Mitchell, Brett M. .
PLOS ONE, 2012, 7 (07)