Ultrastructure and histomorphometric analysis of human umbilical cord vessels in preeclampsia: a potential role of VEGF, VEGFR-1 and VEGFR-2

被引:0
|
作者
Almasry, Shaima M. [1 ,2 ]
Elfayomy, Amr K. [3 ,4 ]
Hashem, Hala E. [5 ]
机构
[1] Taibah Univ, Dept Anat, Al Madinah Al Munawarah, Saudi Arabia
[2] Almansoura Univ, Dept Anat & Embryol, Mansoura, Egypt
[3] Taibah Univ, Dept Obstet & Gynecol, Al Madinah Al Munawarah, Saudi Arabia
[4] Zagazig Univ, Dept Obstet & Gynecol, Zagazig, Egypt
[5] Zagazig Univ, Dept Histol & Cell Biol, Zagazig, Egypt
来源
关键词
VEGF; VEGFR-1; VEGFR-2; umbilical cord vessels; ENDOTHELIAL GROWTH-FACTOR; MUSCLE-CELL PROLIFERATION; FACTOR RECEPTOR-1; VASCULAR-PERMEABILITY; EXPRESSION; ARTERIAL; HYPOXIA; MOUSE;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aim: This study aimed to analyze the ultrastructure and histomorphometric changes of the human umbilical cord vessels of preeclampsia compared to healthy pregnancies and the possible role of vascular endothelial growth factor (VEGF) and its receptors. Materials and Methods: Umbilical cord (UC) specimens were collected between August, 2014 and July, 2015. Histomorphometric analysis of UC vessels was performed utilizing an image analysis system. Cellular localization of VEGF, VEGFR-1 (VEGF receptor-1) and VEGFR-2 (VEGF receptor-2) were examined in immunohistochemically-stained sections of UC from 45 pregnancies with preeclampsia (PE) and 40 healthy pregnancies. Results: Compared with healthy pregnancies, UC venous measurements were significantly higher in PE; total venous area (p<0.001), lumina] venous area (p<0.001) and luminal venous index (p=0.005). Arterial measurements except for the total arterial area were significantly lower in the PE compared to healthy pregnancies, luminal arterial area (p=0.32) and luminal arterial index (p=0.004). Histological and ultrastructural examination of UC from PE revealed discontinuity of vascular endothelium and disorganized edematous widely spaced smooth muscle cells. We demonstrated a significant increase in tissue expression of VEGF in PE (16.6 +/- 0.1) compared to healthy pregnancies (12 +/- 0.8) (p=0.001). Also, significant higher VEGFR-1 expression in PE (20.5 +/- 2.5) compared to healthy pregnancies (9.5 +/- 1.2) (p<0.001) has been observed. However, tissue expression of VEGFR-2 was decreased significantly in PE (10.5 +/- 0.7) compared to healthy pregnancies (13.8 +/- 1.6) (p=0.043). Conclusions: Altered tissue expression of VEGF and its receptors in the UC vessels could play a crucial role in disturbing the UC vascular endothelium, smooth muscles and measurements and this may underlie the existence of preeclampsia.
引用
收藏
页码:681 / 689
页数:9
相关论文
共 50 条
  • [41] Selective Imaging of VEGFR-1 and VEGFR-2 Using 89Zr-Labeled Single-Chain VEGF Mutants
    Meyer, Jan-Philip
    Edwards, Kimberly J.
    Kozlowski, Paul
    Backer, Marina V.
    Backer, Joseph M.
    Lewis, Jason S.
    JOURNAL OF NUCLEAR MEDICINE, 2016, 57 (11) : 1811 - 1816
  • [42] Intratumoral Poems and Expression of VEGF, VEGFR-1 and VEGFR-2 in different subtypes of primary cutaneous B-cell lymphoma
    Wobser, Marion
    Siedel, Claudia
    Broecker, Eva-Bettina
    Goebeler, Matthias
    Houben, Roland
    Geissinger, Eva
    JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2012, 10 (09): : 676 - 676
  • [43] HIF-1α、VEGF、VEGFR-1、VEGFR-2在稽留流产患者绒毛组织中的表达
    王玲
    赵卫东
    安徽医科大学学报, 2015, 50 (02) : 227 - 231
  • [44] Wogonin inhibits IL-6-induced angiogenesis via down-regulation of VEGF and VEGFR-1, not VEGFR-2
    Lin, Chiu-Mei
    Chang, Hang
    Chen, Yeh-Hsu
    Wu, I-Hsing
    Chiu, Jen-Hwey
    PLANTA MEDICA, 2006, 72 (14) : 1305 - 1310
  • [45] Glioma cells enhance endothelial progenitor cell angiogenesis via VEGFR-2, not VEGFR-1
    Zhang, Junxia
    Zhao, Peng
    Fu, Zhen
    Chen, Xiaolei
    Liu, Ning
    Lu, Ailin
    Li, Rui
    Shi, Lei
    Pu, Peiyu
    Kang, Chunsheng
    You, Yongping
    ONCOLOGY REPORTS, 2008, 20 (06) : 1457 - 1463
  • [46] Neutralizing MoAb to VEGF receptors inhibit proliferation and migration of a subset of human leukemias through interaction with VEGFR-2(KDR) and VEGFR-1(FLT-1).
    Dias, S
    Lane, WJ
    Wu, Y
    Choy, M
    Peichev, M
    Chadburn, A
    Hyjeck, E
    Roboz, G
    Hicklin, D
    Witte, L
    Rafii, S
    BLOOD, 1999, 94 (10) : 620A - 620A
  • [47] 尖锐湿疣组织VEGFR-1和VEGFR-2的水平检测
    姚亚琼
    蔡丙杰
    尹光文
    中国皮肤性病学杂志, 2008, 22 (12) : 718 - 720
  • [48] Expression of Vascular Endothelial Growth Factor Receptor 1(VEGFR-1), but not VEGFR-2 in Activated T Lymphocytes and Its Function in Response to VEGF
    Shin, Jin Young
    Kim, Jung Sik
    Kim, Bongi
    Yun, Il Hee
    Park, Chung Gyo
    JOURNAL OF IMMUNOLOGY, 2007, 178
  • [49] Lymphoma-Expressed VEGF-a,VEGFR-1, VEGFR-2, and Microvessel Density Are Not Predictive of Overall Survival in Follicular Lymphoma.
    Gratzinger, Dita
    Zhao, S.
    Ai, Weiyun
    Tibshirani, Robert
    Levy, Ronald
    Natkunam, Y.
    BLOOD, 2008, 112 (11) : 1290 - 1290
  • [50] Basal and squamous cell carcinomas: Differences in the vasculature, vascular endothelial growth factor (VEGF), VEGF receptor-1 (VEGFR-1) and VEGF receptor-2 (VEGFR-2) expression
    Tsiatoura, Amalia
    Batistatou, Anna
    Zioga, Aikaterini
    Agnantis, Niki J.
    Stefanou, Dimitrios
    VIRCHOWS ARCHIV, 2007, 451 (02) : 536 - 537