TY - JOUR
T1 - Pre-eclampsia onset and SPARC: A possible involvement in placenta development
AU - Tossetta, Giovanni
AU - Fantone, Sonia
AU - Giannubilo, Stefano R.
AU - Marinelli Busilacchi, Elena
AU - Ciavattini, Andrea
AU - Castellucci, Mario
AU - Di Simone, Nicoletta
AU - Mattioli-Belmonte, Monica
AU - Marzioni, Daniela
PY - 2019
Y1 - 2019
N2 - Pre‐eclampsia (PE) is a multisystem disorder commonly diagnosed in the latter half of
pregnancy and it is a leading cause of intrauterine fetal growth retardation (IUGR).
The aim of this study was to investigate the localization and the role of SPARC,
secreted protein acidic, and rich in cysteine, in PE and PE–IUGR placentas in
comparison with normal placentas. SPARC was mainly expressed in the villous and
extravillous cytotrophoblastic cells in first trimester, whereas in PE, PE–IUGR and at
term placentas, SPARC immunostaining was visible in both cytotrophoblastic cells
and syncytiotrophoblast. SPARC expression significantly decreased in normal
placenta from first to third trimester and a further significant reduction was
demonstrated in PE and PE–IUGR. The latter downregulation of SPARC depends on
hypoxic condition as shown by in vitro models. In conclusion, SPARC can play a
pivotal role in PE and PE–IUGR onset and it should be considered as a key molecule
for future investigations in such pathologies.
AB - Pre‐eclampsia (PE) is a multisystem disorder commonly diagnosed in the latter half of
pregnancy and it is a leading cause of intrauterine fetal growth retardation (IUGR).
The aim of this study was to investigate the localization and the role of SPARC,
secreted protein acidic, and rich in cysteine, in PE and PE–IUGR placentas in
comparison with normal placentas. SPARC was mainly expressed in the villous and
extravillous cytotrophoblastic cells in first trimester, whereas in PE, PE–IUGR and at
term placentas, SPARC immunostaining was visible in both cytotrophoblastic cells
and syncytiotrophoblast. SPARC expression significantly decreased in normal
placenta from first to third trimester and a further significant reduction was
demonstrated in PE and PE–IUGR. The latter downregulation of SPARC depends on
hypoxic condition as shown by in vitro models. In conclusion, SPARC can play a
pivotal role in PE and PE–IUGR onset and it should be considered as a key molecule
for future investigations in such pathologies.
KW - IUGR
KW - hypoxia
KW - IUGR
KW - hypoxia
UR - http://hdl.handle.net/10807/128693
U2 - 10.1002/jcp.27344
DO - 10.1002/jcp.27344
M3 - Article
SN - 0021-9541
VL - 234
SP - 6091
EP - 6098
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
ER -