Hormonal regulation of connexin-43 in baboon corpora lutea

被引:20
|
作者
Khan-Dawood, FS [1 ]
Yang, J [1 ]
Dawood, MY [1 ]
机构
[1] Univ Texas, Sch Med, Dept Obstet Gynecol & Reprod Sci, Hlth Sci Ctr,Div Reprod Endocrinol, Houston, TX 77030 USA
关键词
D O I
10.1677/joe.0.1570405
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The synthesis and secretion of progesterone in the corpus luteum are regulated by both endocrine and paracrine/autocrine factors which affect the steroidogenic cells. Evidence suggests that these cells communicate via cell-cell junctional proteins, the connexins. Previously we have shown that connexin-43 is expressed ill both human and baboon (Papio hamadryus anubis) corpora lutea, with differential expression throughout luteal development, but is not detectable in corpora albicantia. We have examined the effect of human chorionic gonadotropin (hCG), oxytocin, clomiphene citrate and the anti-progesterone onapristone on expression of connexin-43 protein in the early luteal phase 1-5 days after the mid-cycle luteinizing hormone (LH) surge (LH+ 1-5 days), the mid-luteal phase 6-10 days after the LH surge (LH+6-10 days), and the late luteal phase 11-15 days after the LH surge (LH+11-15 days) in corpora lutea obtained from normal adult cycling females. Connexin-43 was localized by immunohistochemistry in cultured cells from all the three stages. Western blot analysis of die treated cells indicated the presence of two bands at 43 and 45 kDa. The band at 45 kDa was found to be phosphorylated connexin-43, indicating the presence of functional gap junctions, hCG (10 IU/mL) stimulated the expression of connexin-43 throughout luteal development; however, maximum expression occurred in the early luteal phase with a significantly greater expression of the non-phosphorylated protein. In contrast, in the mid-luteal phase, the expression of the phosphorylated protein was predominant. Oxytocin (200 mU/ml) also stimulated connexin-43 expression throughout luteal development with similar effects on the phosphorylated and non-phosphorylated protein in the early and mid-luteal phase; however, compared with hCG, oxytocin had a greater effect on mid-luteal phase connexin-43 expression. In the presence of both hCG and oxytocin, the expression of connexin-43 was significantly higher than the control only in the late luteal phase. Both clomiphene citrate and onapristone suppressed connexin-43 expression, and concomitant addition of hCG did not counteract their effect.. In the context of our previous studies, it is concluded that, together with LH/hCG and the steroid hormones, oxytocin is involved in cell-cell contact-dependent communication in the corpus luteum.
引用
收藏
页码:405 / 414
页数:10
相关论文
共 50 条
  • [41] Regulation of connexin-43 gap junctional intercellular communication by mitogen-activated protein kinase
    Warn-Cramer, BJ
    Cottrell, GT
    Burt, JM
    Lau, AF
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) : 9188 - 9196
  • [42] Up-regulation of myocardial connexin-43 is involved in compensatory response of the heart to acute injury
    Tribulova, N.
    Viczenczova, C.
    Kura, B.
    Chaudagar, K. K.
    Bacova, B. Szeiffova
    Benova, T. Egan
    Knezl, V.
    Barancik, M.
    Ravingerova, T.
    Slezak, J.
    CARDIOVASCULAR RESEARCH, 2018, 114 : S67 - S67
  • [43] PHORBOL ESTER INDUCES PHOSPHORYLATION AND DOWN-REGULATION OF CONNEXIN-43 IN WB-CELLS
    OH, SY
    GRUPEN, CG
    MURRAY, AW
    BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1094 (02) : 243 - 245
  • [44] HORMONAL-REGULATION OF CONNEXIN43 EXPRESSION AND FUNCTION IN OSTEOBLASTIC CELLS
    CIVITELLI, R
    WARLOW, PM
    NELSON, T
    BEYER, EC
    STEINBERG, TH
    JOURNAL OF BONE AND MINERAL RESEARCH, 1993, 8 : S163 - S163
  • [45] INHIBITION OF GLYCOSYLATION INDUCES FORMATION OF OPEN CONNEXIN-43 CELL-TO-CELL CHANNELS AND PHOSPHORYLATION AND TRITON X-100 INSOLUBILITY OF CONNEXIN-43
    WANG, YJ
    MEHTA, PP
    ROSE, B
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) : 26581 - 26585
  • [46] Array analysis of gene expression in connexin-43 null astrocytes
    Iacobas, DA
    Maldonado, MU
    Iacobas, S
    Scemes, E
    Spray, DC
    PHYSIOLOGICAL GENOMICS, 2003, 15 (03) : 177 - 190
  • [47] IDENTIFICATION OF CONNEXIN-43, A GAP JUNCTION PROTEIN, OF HUMAN EPIDERMIS
    MEDA, P
    MASGRAU, E
    SAURAT, JH
    SALOMON, D
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (04) : 480 - 480
  • [48] Identification of the PKC-epsilon binding domain on Connexin-43
    Dang, XT
    Kardami, E
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 36 (04) : 623 - 623
  • [49] Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions
    Fasciani, Ilaria
    Pluta, Paula
    Gonzalez-Nieto, Daniel
    Martinez-Montero, Paloma
    Molano, Jesus
    Paino, Carlos L.
    Millet, Oscar
    Barrio, Luis C.
    GLIA, 2018, 66 (11) : 2340 - 2352
  • [50] Phosphorylation of a specific serine on connexin-43 affects cardiomyocyte proliferation
    Doble, BW
    Dang, XT
    Jin, Y
    Cattini, PA
    Kardami, E
    MOLECULAR BIOLOGY OF THE CELL, 2000, 11 : 224A - 225A