Syndecan-4 expression is associated with follicular atresia in mouse ovary

被引:35
作者
Ishiguro, K
Kojima, T
Taguchi, O
Saito, H
Muramatsu, T
Kadomatsu, K
机构
[1] Nagoya Univ, Sch Med, Dept Biochem, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Aichi Canc Ctr, Res Inst, Lab Expt Pathol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[3] Nagoya Univ, Sch Med, Dept Internal Med 1, Nagoya, Aichi 4668550, Japan
关键词
D O I
10.1007/s004180050388
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ovarian granulosa cells synthesize heparan sulfate proteoglycans (HSPGs), that have anticoagulant properties. Moreover, HSPGs greatly increase in the granulosa cells during follicular atresia. However, the species of ovarian HSPGs have not yet been identified. Syndecan-4 (ryudocan, amphiglycan) is a membrane-spanning HSPG and a member of the syndecan family. Herein, we demonstrate that syndecan-4 is expressed in the granulosa cells of type 4-5b follicles and, most intensely, in those of the atretic follicles in the mouse ovary, as revealed by in situ hybridization. There is no relationship between syndecan-4 expression and age or sexual cycle stage. Compared with syndecan-4 expression, syndecan-1 and -3 are expressed more abundantly in postovulatory follicles and the corpora lutea, but less in the type 4-5b follicles and much less in the atretic follicles. Immunohistochemistry also demonstrates syndecan-4 expression in atretic follicles with apoptosis. The present study has revealed the distinct modes of expression of the syndecan family members, and the association of syndecan-4 expression and apoptosis in ovarian atretic follicles.
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页码:25 / 33
页数:9
相关论文
共 61 条
  • [11] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [12] Hormonal regulation of apoptosis in early antral follicles: Follicle-stimulating hormone as a major survival factor
    Chun, SY
    Eisenhauer, KM
    Minami, S
    Billig, H
    Perlas, E
    Hsueh, AJW
    [J]. ENDOCRINOLOGY, 1996, 137 (04) : 1447 - 1456
  • [13] Syndecan-4 is a primary-response gene induced by basic fibroblast growth factor and arterial injury in vascular smooth muscle cells
    CizmeciSmith, G
    Langan, E
    Youkey, J
    Showalter, LJ
    Carey, DJ
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (01) : 172 - 180
  • [14] Couchman JR, 1996, J CELL BIOCHEM, V61, P578, DOI 10.1002/(SICI)1097-4644(19960616)61:4<578::AID-JCB11>3.0.CO
  • [15] 2-C
  • [16] DAVID G, 1993, DEVELOPMENT, V119, P841
  • [17] MOLECULAR-CLONING OF AMPHIGLYCAN, A NOVEL INTEGRAL MEMBRANE HEPARAN-SULFATE PROTEOGLYCAN EXPRESSED BY EPITHELIAL AND FIBROBLASTIC CELLS
    DAVID, G
    VANDERSCHUEREN, B
    MARYNEN, P
    CASSIMAN, JJ
    VANDENBERGHE, H
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 118 (04) : 961 - 969
  • [18] Syndecan-1 is a multifunctional regulator of myeloma pathobiology: Control of tumor cell survival, growth, and bone cell differentiation
    Dhodapkar, MV
    Abe, E
    Theus, A
    Lacy, M
    Langford, JK
    Barlogie, B
    Sanderson, RD
    [J]. BLOOD, 1998, 91 (08) : 2679 - 2688
  • [19] INDUCED EXPRESSION OF SYNDECAN IN HEALING WOUNDS
    ELENIUS, K
    VAINIO, S
    LAATO, M
    SALMIVIRTA, M
    THESLEFF, I
    JALKANEN, M
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 114 (03) : 585 - 595
  • [20] Time-dependent increases in syndecan-1 and fibroglycan messenger RNA expression in the infarct zone after experimentally induced myocardial infarction in rats
    Endo, C
    Kusachi, S
    Ninomiya, Y
    Yamamoto, K
    Murakami, M
    Murakami, T
    Shinji, T
    Koide, N
    Kondo, J
    Tsuji, T
    [J]. CORONARY ARTERY DISEASE, 1997, 8 (3-4) : 155 - 161