Jj. Timmerman et al., DIFFERENTIAL EXPRESSION OF COMPLEMENT COMPONENTS IN HUMAN FETAL AND ADULT KIDNEYS, Kidney international, 49(3), 1996, pp. 730-740
Various studies have shown that complement components are synthesized
by renal cells and that mRNA for a number of complement components is
detectable in renal tissue. The present study shows that complement pr
oteins are present both in fetal and adult human kidneys. The localiza
tion of the complement components was compared with the localization o
f other proteins for which specific expression in defined renal cell t
ypes is known from the literature. In adult human kidneys C3, factor B
and factor H were detected in the mesangial area by immunohistochemis
try, whereas C2 and C4 were present in the proximal tubuli. In fetal k
idneys C3 and factor B were expressed in glomeruli of kidneys of 11 we
eks of gestation. In kidneys of 13 to 19 weeks of gestation no stainin
g for C3 was found in the glomerulus, whereas for factor B glomerular
staining was found in all fetal kidneys examined. Factor B was also de
tected in fetal tubuli and in the interstitium. Factor H was expressed
in fetal tubuli starting at 13 weeks of gestation. For both C3 and C2
weak tubular staining was found in all fetal kidneys investigated. C4
could not be detected in any of the fetal kidneys. While not all the
complement proteins investigated were detectable by immunohistochemist
ry, by RT-PCR analysis, mRNA expression for C3, factor B, factor H, C2
and C4 was found in all adult and fetal renal tissue. The finding of
mRNA for the complement components in the fetal and the adult kidneys
indicates that local synthesis of complement occurs both in the adult
and in the fetal kidney. Next to the in situ expression of complement
components in fetal kidneys the synthesis of complement proteins in vi
tro by fetal renal cells was investigated. Four different primary mesa
ngial cell lines were shown to synthesize all complement proteins inve
stigated. Although a specific role for complement during the developme
nt of the kidney is not known, it is possible that certain complement
components may play a role during renal differentiation.