Derangements in Endothelial Cell-to-Cell Junctions Involved in the Pathogenesis of Hypercholesterolemia-Induced Erectile Dysfunction

被引:23
|
作者
Ryu, Ji-Kan [1 ,2 ]
Zhang, Lu Wei [1 ,2 ]
Jin, Hai-Rong [1 ,2 ]
Piao, Shuguang [1 ,2 ]
Choi, Min Ji [1 ,2 ]
Tuvshintur, Buyankhuu [1 ,2 ]
Tumurbaatar, Munkhbayar [1 ,2 ]
Shin, Sun Hwa [1 ,2 ]
Han, Jee-Young [3 ]
Kim, Woo Jean [1 ,2 ]
Suh, Jun-Kyu [1 ,2 ]
机构
[1] Inha Univ, Sch Med, Dept Urol, Inchon 400711, South Korea
[2] Inha Univ, Sch Med, Natl Res Lab Regenerat Sexual Med, Inchon 400711, South Korea
[3] Inha Univ, Sch Med, Dept Pathol, Inchon 400711, South Korea
来源
JOURNAL OF SEXUAL MEDICINE | 2009年 / 6卷 / 07期
关键词
Erectile Dysfunction; Elevated Cholesterol; Penis; Endothelium; Junction; RISK-FACTORS; VASCULAR-PERMEABILITY; ADHERENS JUNCTIONS; RAT MODEL; CADHERIN; VEGF; ANGIOGENESIS; EXPRESSION; PECAM-1; GENE;
D O I
10.1111/j.1743-6109.2009.01275.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction. Endothelial cell-to-cell junctions are crucial for vascular formation, networking, and remodeling of blood vessels as well as for inducing and integrating intracellular signals. Aim. We investigated the differential expression and distribution of endothelial cell-to-cell junction proteins in the penis of mice with hypercholesterolemia-induced erectile dysfunction. Methods. Two-month-old C57BL/6J mice were fed a diet containing 4% cholesterol and 1% cholic acid, and age-matched control animals were fed a normal diet, for 3 months. We performed dual priming oligonucleotide (DPO)-based multiplex polymerase chain reaction (PCR) (Seegene, Seoul, Korea) to screen the differential gene expression of 21 endothelial cell-to-cell junctions. Main Outcome Measures. At 5 months, erectile function was measured by electrical stimulation of the cavernous nerve, and the penis was harvested and stained with antibody to claudin-5, vascular endothelial (VE)-cadherin, and platelet/endothelial cell adhesion molecule (PECAM)-1 (N = 8 per group). Cavernous specimens from a separate group of animals were used for claudin-5, VE-cadherin, and PECAM-1 reverse transcriptase-PCR and Western blot analysis. Results. Erectile function was significantly lower in hypercholesterolemic mice than in controls. DPO-based multiplex PCR revealed a profound decrease in the gene expression of endothelium-specific cell-to-cell junction proteins, including claudin-5, VE-cadherin, and PECAM-1, in hypercholesterolemic mice compared with that in controls. The expression of claudin-5, VE-cadherin, and PECAM-1 protein evaluated by Western blot or immunohistochemistry was significantly lower in hypercholesterolemic mice than in controls. These endothelial cell-to-cell junction proteins were more sparsely distributed in the endothelium of cavernous sinusoids than in the endothelium of cavernous artery and dorsal blood vessels. Conclusion. Down-regulation of the endothelial cell-to-cell junctions and decreased endothelial content in the corpus cavernosum might play a major role in the deterioration of erectile function in hypercholesterolemic mice. Ryu J-K, Zhang LW, Jin H-R, Piao S, Choi MJ, Tuvshintur B, Tumurbaatar M, Shin SH, Han J-Y, Kim WJ, and Suh J-K. Derangements in endothelial cell-to-cell junctions involved in the pathogenesis of hypercholesterolemia-induced erectile dysfunction. J Sex Med 2009;6:1893-1907.
引用
收藏
页码:1893 / 1907
页数:15
相关论文
共 50 条
  • [1] DERANGEMENTS IN ENDOTHELIAL CELL-TO-CELL JUNCTIONS INVOLVE IN THE PATHOGENESIS OF HYPERCHOLESTEROLEMIA-INDUCED ERECTILE DYSFUNCTION
    Jin, Hai-Rong
    Ryu, Ji-Kan
    Zhang, Lu Wei
    Piao, Shuguang
    Choi, Min Ji
    Tuvshintur, Buyankhuu
    Tumurbaatar, Munkhbayar
    Shin, Sun Hwa
    Han, Jee-Young
    Kim, Woo Jean
    Suh, Jun-Kyu
    JOURNAL OF UROLOGY, 2009, 181 (04): : 239 - 239
  • [2] A mouse model of hypercholesterolemia-induced erectile dysfunction
    Xie, Donghua
    Odronic, Shelly I.
    Wu, Feihua
    Pippen, Anne M.
    Donatucci, Craig F.
    Annex, Brian H.
    JOURNAL OF SEXUAL MEDICINE, 2007, 4 (04): : 898 - 907
  • [3] Roles of platelet and endothelial cell COX-1 in hypercholesterolemia-induced microvascular dysfunction
    Tailor, Anitaben
    Wood, Katherine C.
    Wallace, John L.
    Specian, Robert D.
    Granger, D. Neil
    AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 293 (06): : H3636 - H3642
  • [4] ENDOTHELIAL CELL-TO-CELL JUNCTIONS
    DEJANA, E
    CORADA, M
    LAMPUGNANI, MG
    FASEB JOURNAL, 1995, 9 (10): : 910 - 918
  • [5] Role of lymphocytes in hypercholesterolemia-induced endothelial cell adhesion.
    Stokes, K
    Lea, R
    Granger, DN
    FASEB JOURNAL, 1999, 13 (04): : A89 - A89
  • [6] Endothelial cell-to-cell junctions.
    Dejana, E
    JOURNAL OF VASCULAR RESEARCH, 2005, 42 : 20 - 20
  • [7] Membrane Cholesterol Interactions with Proteins in Hypercholesterolemia-Induced Endothelial Dysfunction
    Fancher, Ibra S.
    Levitan, Irena
    CURRENT ATHEROSCLEROSIS REPORTS, 2023, 25 (09) : 535 - 541
  • [8] REVERSAL OF HYPERCHOLESTEROLEMIA-INDUCED ENDOTHELIAL DYSFUNCTION BY L-ARGININE
    RUBANYI, GM
    CIRCULATION, 1991, 83 (03) : 1118 - 1120
  • [9] Membrane Cholesterol Interactions with Proteins in Hypercholesterolemia-Induced Endothelial Dysfunction
    Ibra S. Fancher
    Irena Levitan
    Current Atherosclerosis Reports, 2023, 25 : 535 - 541
  • [10] Interferon-γ contributes to hypercholesterolemia-induced leukocyte endothelial cell adhesion.
    Clements, KP
    Stokes, KY
    Clanton, EC
    Granger, DN
    FASEB JOURNAL, 2001, 15 (04): : A120 - A120