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Vascular endothelial growth factor stimulates embryonic urinary bladder development in organ culture
Author(s) -
BURGU BERK,
MCCARTHY LIAM S.,
SHAH Vanita,
LONG DAVID A.,
WILCOX DUNCAN T.,
WOOLF ADRIAN S.
Publication year - 2006
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/j.1464-410x.2006.06215.x
Subject(s) - vascular endothelial growth factor , cd31 , organ culture , biology , angiogenesis , embryonic stem cell , urothelium , vascular endothelial growth factor a , microbiology and biotechnology , growth factor , urinary bladder , stromal cell , receptor , medicine , endocrinology , cancer research , urinary system , in vitro , vegf receptors , biochemistry , gene
OBJECTIVES To determine whether vascular endothelial growth factor A (VEGF) and its receptors are expressed during bladder development in mice when capillaries are forming, and whether exogenous VEGF might enhance the growth of endothelia and other types of bladder cells, using an embryonic organ‐culture model. MATERIALS AND METHODS Whole bladders from wild‐type mice, at embryonic day (E) 14, were grown in serum‐free organ culture in an air/5% CO 2 atmosphere; some cultures were supplemented with VEGF and/or with VEGF receptor 1/Fc chimera (VEGFR1/Fc), which blocks VEGF bioactivity. Organs were harvested after 6 days and the expression of VEGF and related molecules assessed using immunohistochemistry. RESULTS VEGF, VEGFR1 and VEGFR2 positive cells were immunodetected in E14 and E18 bladders. Exogenous VEGF increased whole‐organ growth, as assessed by explant areas, total cell numbers, DNA and protein content; proliferation was enhanced, and apoptosis decreased, in urothelium and surrounding tissues. VEGF also increased the proportions of cells expressing endothelial (CD31) and smooth muscle (α smooth muscle actin) markers. VEGFR1/Fc blocked the growth‐enhancing effects of exogenous VEGF. CONCLUSIONS In organ culture, exogenous VEGF not only stimulated embryonic bladder endothelial cells but also strikingly enhanced the growth of the whole organ. Whether the effects of VEGF on diverse bladder cell populations are direct or indirect requires further investigation. The finding that VEGF protein is present in embryonic bladders in vivo raises the possibility that it has similar actions during normal development. The results also illuminate the pathobiology of certain bladder diseases in which VEGF levels have been shown to be increased.