Cell-cycle control in cell-biomaterial interactions: Expression of p53 andKi67 in human umbilical vein endothelial cells in direct contact and extract testing of biomaterials
Tg. Van Kooten et al., Cell-cycle control in cell-biomaterial interactions: Expression of p53 andKi67 in human umbilical vein endothelial cells in direct contact and extract testing of biomaterials, J BIOMED MR, 52(1), 2000, pp. 199-209
Current biocompatibility testing involves the demonstration of cell prolife
ration, which is usually interpreted as a sign of positive biocompatibility
when the materials sustain cell proliferation. As the field of biomaterial
s research is rapidly moving toward tissue-engineered devices and hybrid or
gans, control of cell function has become a main topic. Cell function, whic
h involves specific differentiation pathways, cannot be separated from cell
-cycle control. The study of cell-cycle control is an important extension o
f routine proliferation assays and has extensive roots in developmental and
tumor biology. We studied the expression of the tumour suppressor gene p53
and the proliferation-associated antigen Ki67 of endothelial cells in resp
onse to biomaterial contact. Cells were seeded in six- or 24-well plates, i
n which one or three 12-mm-diameter biomaterial disks were laid down. After
48- and 72-h incubation periods, cells were processed for flow cytometry,
immunofluorescence, or Western blotting. The following materials were used:
titanium, NiCr alloy, and CoCr alloy. Cells were also exposed to 24-h (ISO
-norm) extracts in 25-cm(2) culture flasks (600,000 cells) for 24 and 48 h.
For extract testing, serially diluted Ni-ion suspensions were also used. H
uman umbilical vein endothelial cells adhered to metal surfaces and started
forming a monolayer within 3 days. Ki67 expression was positive in more th
an 60% after 2 days and decreased markedly after 3 days of adhesion. During
this time cells developed focal contacts and produced a fibronectin matrix
. p53 expression could be demonstrated with Western blotting and flow cytom
etry, but not with immunofluorescence. Differences due to both culturing ti
me and material were found in expression patterns with both methods. Invers
e correlations between Ki67 and p53 expression were detected, which are pro
bably based on culture kinetics. The results indicate that expression of p5
3 and also Ki67 is clearly influenced by biomaterials in direct contact tes
ting, despite the absence of obvious morphological differences. The p53 mar
ker can be used for defining cell function in more detail, although the cor
relation with specific physiological function has still to be clarified. (C
) 2000 John Wiley & Sons, Inc.