C. Doucet et al., LIPOPROTEIN[A] IN THE CHIMPANZEE - RELATIONSHIP OF APO[A] PHENOTYPE TO ELEVATED PLASMA LP[A] LEVELS, Journal of lipid research, 35(2), 1994, pp. 263-270
Several studies have documented the presence of Lp[a] in nonhuman prim
ates. However, data are lacking in great apes such as the chimpanzee.
We have studied the quantitative distribution of Lp[a], as well as the
frequency of apo[a] phenotypes, in a population of chimpanzees living
in Gabon. Monoclonal antibody 14A12, directed against human apo[a], f
ailed to recognize chimpanzee Lp[a]. Therefore, Lp[a] was assayed usin
g an ELISA involving two polyclonal antibodies, an anti-human apo[a] a
nd an anti-human apoB-100. Under these conditions, Lp[a] was detected
in each of 28 animals. The plasma level of Lp[a] was found to be highl
y skewed toward elevated values: the mean Lp[a] level was 0.61 mg/ml (
SD 0.45) as compared to 0.18 mg/ml (SD 0.16) in a normal Caucasian pop
ulation (P < 0.0001). Phenotypes for apo[a] were identified by SDS-aga
rose-gel electrophoresis, followed by immunoblotting and detection by
chemiluminescence. Seventeen different isoforms (ranging from 440 to 9
20 kDa) were found among all the animals as compared to 19 (540 to 960
kDa) in a human population of equivalent number. However, the distrib
ution of apo[a] phenotypes was distinct between these populations. Thu
s isoforms of low molecular mass occurred with greater frequency in ch
impanzee as compared to humans. In both populations, a strong inverse
correlation between Lp[a] levels and apo[a] isoform sizes was found in
chimpanzees (r = -0.48; P < 0.01) and in man (r = -0.68; P < 0.0002).
Clearly then, chimpanzees differ not only from humans, but also from
other nonhuman primates, such as the cynomolgus monkey and baboon, in
both the distribution of their Lp[a] levels and the frequency of apo[a
] isoforms.