Open AccessFunctional Differences Between Placental Micro‐ and Macrovascular Endothelial Colony‐Forming Cells
Author(s) -
Solomon Ioana,
O'Reilly Megan,
Ionescu Lavinia,
Alphonse Rajesh S.,
Rajabali Saima,
Zhong Shumei,
Vadivel Arul,
Shelley W. Chris,
Yoder Mervin C.,
Thébaud Bernard
Publication year - 2016
Publication title -
stem cells translational medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.781
H-Index - 71
eISSN - 2157-6580
pISSN - 2157-6564
DOI - 10.5966/sctm.2014-0162
Subject(s) - matrigel , cd146 , preeclampsia , placenta , cd31 , vasculogenesis , endoglin , fetal membrane , immunology , biology , andrology , stem cell , microbiology and biotechnology , progenitor cell , medicine , fetus , cd34 , angiogenesis , cancer research , pregnancy , immunohistochemistry , genetics
Alterations in the development of the placental vasculature can lead to pregnancy complications, such as preeclampsia. Currently, the cause of preeclampsia is unknown, and there are no specific prevention or treatment strategies. Further insight into the placental vasculature may aid in identifying causal factors. Endothelial colony‐forming cells (ECFCs) are a subset of endothelial progenitor cells capable of self‐renewal and de novo vessel formation in vitro. We hypothesized that ECFCs exist in the micro‐ and macrovasculature of the normal, term human placenta. Human placentas were collected from term pregnancies delivered by cesarean section ( n = 16). Placental micro‐ and macrovasculature was collected from the maternal and fetal side of the placenta, respectively, and ECFCs were isolated and characterized. ECFCs were CD31 + , CD105 + , CD144 + , CD146 + , CD14 − , and CD45 − , took up 1,1′‐dioctadecyl‐3,3,3′,3′‐tetramethyl‐indocarbocyanine perchlorate‐labeled acetylated low‐density lipoprotein, and bound Ulex europaeus agglutinin 1. In vitro, macrovascular ECFCs had a greater potential to generate high‐proliferative colonies and formed more complex capillary‐like networks on Matrigel compared with microvascular ECFCs. In contrast, in vivo assessment demonstrated that microvascular ECFCs had a greater potential to form vessels. Macrovascular ECFCs were of fetal origin, whereas microvascular ECFCs were of maternal origin. ECFCs exist in the micro‐ and macrovasculature of the normal, term human placenta. Although macrovascular ECFCs demonstrated greater vessel and colony‐forming potency in vitro, this did not translate in vivo, where microvascular ECFCs exhibited a greater vessel‐forming ability. These important findings contribute to the current understanding of normal placental vascular development and may aid in identifying factors involved in preeclampsia and other pregnancy complications. Significance This research confirms that resident endothelial colony‐forming cells (ECFCs) exist in the micro‐ and macrovasculature of the normal, term human placenta. Their isolation from two different anatomical locations yields two functionally different ECFC populations. Investigation of these ECFC populations during placental pathologies, such as preeclampsia, may lead to a better understanding of the disease process and aid in developing new therapies.