Change in VEGF Expression in Mouse Mammary Gland during Reproductive Cycle

被引:5
作者
Islam, Mohammad Saiful [1 ]
Matsumoto, Mitsuharu [1 ]
Ishida, Rina [1 ]
Oka, Tatsuzo [2 ]
Kanouchi, Hiroaki [2 ]
机构
[1] Kagoshima Univ, Dept Vet Med, Lab Vet Anat, Fac Agr, Kagoshima 8900065, Japan
[2] Kagoshima Univ, Dept Vet Med, Lab Vet Pathobiol, Fac Agr, Kagoshima 8900065, Japan
基金
日本学术振兴会;
关键词
immunohistochemistry; mammary gland; mouse; reproductive cycle; VEGF; ENDOTHELIAL GROWTH-FACTOR; NITRIC-OXIDE SYNTHASE; ANGIOGENESIS; BREAST; MILK; PREGNANCY; APOPTOSIS; RECEPTORS; LACTATION; CANCER;
D O I
10.1292/jvms.10-0086
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
During pregnancy, the mammary epithelium and its supporting vasculature undergo extensive growth and proliferation in preparation for lactation, which is thought to be dependent on vascular endothelial growth factor (VEGF). We investigated the expression of VEGF, using immunohistochemistry and immunoblotting, in the mouse mammary gland during the reproductive cycle. Immunohistochemical studies localized VEGF protein predominantly in the cytoplasm of the mammary epithelium and revealed it to be strongly expressed in late pregnancy and early lactation. In addition, immunoblot analysis revealed a 45-kD VEGF band, corresponding to the homodimer of the VEGF-A(164) isoform, with increased expression towards the end of pregnancy but no additional increase with the onset of lactation. As the post-lactation period advanced, a dramatic decrease in VEGF was observed in the regressed mammary epithelium. The expression of VEGF suggests that mammary epithelium-derived VEGF may be involved in pregnancy-associated mammary growth and differentiation and angiogenesis, and regulate vascular permeability during lactation in an autocrine or paracrine manner.
引用
收藏
页码:1159 / 1163
页数:5
相关论文
共 25 条
[1]   Apoptosis in the estrous and menstrual cycles [J].
Andres, AC ;
Strange, R .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 1999, 4 (02) :221-228
[2]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[3]  
Djonov V, 2001, MICROSC RES TECHNIQ, V52, P182, DOI 10.1002/1097-0029(20010115)52:2<182::AID-JEMT1004>3.0.CO
[4]  
2-M
[5]   The biology of VEGF and its receptors [J].
Ferrara, N ;
Gerber, HP ;
LeCouter, J .
NATURE MEDICINE, 2003, 9 (06) :669-676
[6]   Predominant role of endothelial nitric oxide synthase in vascular endothelial growth factor-induced angiogenesis and vascular permeability [J].
Fukumura, D ;
Gohongi, T ;
Kadambi, A ;
Izumi, Y ;
Ang, J ;
Yun, CO ;
Buerk, DG ;
Huang, PL ;
Jain, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2604-2609
[7]   Regulation of endothelium-derived nitric oxide production by the protein kinase Akt [J].
Fulton, D ;
Gratton, JP ;
McCabe, TJ ;
Fontana, J ;
Fujio, Y ;
Walsh, K ;
Franke, TF ;
Papapetropoulos, A ;
Sessa, WC .
NATURE, 1999, 399 (6736) :597-601
[8]   The mechanisms on apoptosis by inhibiting VEGF expression in human breast cancer cells [J].
Ge, Yin-Lin ;
Zhang, Xiao ;
Zhang, Jin-Yu ;
Hou, Lin ;
Tian, Run-Hua .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2009, 9 (04) :389-395
[9]   Information networks in the mammary gland [J].
Hennighausen, L ;
Robinson, GW .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (09) :715-725
[10]   Transcriptional regulation of vascular endothelial growth factor expression in epithelial and stromal cells during mouse mammary gland development [J].
Hovey, RC ;
Goldhar, AS ;
Baffi, J ;
Vonderhaar, BK .
MOLECULAR ENDOCRINOLOGY, 2001, 15 (05) :819-831