The Biological and Immunological Characterization of Inhibin A and B Forms in Human Follicular Fluid and Plasma1
D. M. Robertson,
N. Cahir,
J. K. Findlay,
H. G. Burger and
N. Groome
Prince Henrys Institute of Medical Research (D.M.R., N.C.,
J.K.F., H.G.B.), Monash Medical Centre, Clayton Victoria 3168,
Australia and Oxford Brookes University (N.G.), Oxford, OX3 OBP United
Kingdom
Address all correspondence and requests for reprints to: David Robertson, Ph.D., Prince Henrys Institute of Medical Research, Monash Medical Centre, Clayton Victoria 3168, Australia.
In a previous study (see Ref. 7), the molecular weight distributionof
inhibin activity in fractionated human follicular fluid (hFF)and human
male and female plasma/serum was determined by invitro
bioassay using ovine pituitary cells in culture and variousspecific
inhibin A and inhibin -subunit-directed immunoassays.It was shown,
however, that the ovine in vitro bioassay detected
inhibinB poorly. These findings are extended in the present study by
thedetermination of the molecular weight profile of in
vitro bioactivityusing rat pituitary cells, which detects both
inhibin A andB, a specific inhibin B enzyme-linked immunosorbent assay
(ELISA),an RIA detecting the N region of the -subunit, an
-subunit ELISA(Pro-C) directed to the inhibin forms containing
the Pro sequence,and an C subunit immunofluorometric assay that
detects all inhibinforms. The profile in hFF of inhibin in
vitro bioactivity, usingrat pituitary cells in culture,
significantly (P < 0.001)correlated with
in vitro bioactivity using ovine pituitary cells(r
= 0.85), inhibin A immunoactivity (r = 0.70), inhibin B
immunoactivity(r = 0.89), and the combination of inhibin A+B
immunoactivities(r = 0.93), with peaks of activity identified at
66K, 55K, 36Kand 33K, consistent with presumed known mol wt forms of
inhibin.Inhibin B profiles in fractionated serum from women stimulated
withgonadotropins and male plasma consisted of two forms (66K and
36K),whereas inhibin A in female serum included, in addition, the55K
form. These findings indicated that higher molecular weightforms of
inhibin B are present in biological samples, and theirdistribution
differs from that of inhibin A, suggesting a differentialprocessing of
the precursor forms in the circulation. Pro-Cimmunoactivity was
identified in serum samples with prominentpeaks at 36K and 29K (known
Pro-C subunit forms) and not withany high mol wt dimeric forms of
inhibin. If this observationapplies to a wider range of serum samples,
the Pro-C ELISA mayprovide an appropriate and specific assay for
the measurementof free -subunit. To compare immunoactivity levels
between assays,the inhibins A, B, and Pro-C standards were
calibrated in termsof their C subunit content, as determined by an
C subunit immunoassay,with the inhibin B standard containing 60%
of the C subunitcontent compared with either the inhibin A or
Pro-C standard.After adjustments of the various standards for this
differencein C subunit content, a comparison was undertaken of the
combinedlevels of inhibins A, B, and Pro-C immunoactivity across
thehFF and serum chromatograms and compared with levels determinedby
the -subunit-directed immunoassays. A high correlation (r=
0.590.96) was observed, indicating that the -subunit
immunoactivityin serum consists largely of a composite of presumed
known molecularweight forms of inhibins A, B, and Pro-C. It is
concluded that:1) inhibin in vitro bioactivity in hFF
is largely attributedto the presence of 3336K and 5066K forms of
inhibinsA and B; and 2) inhibin -subunit immunoactivity in hFF and
serumis a composite of presumed known forms of inhibin A, inhibinB,
and the -subunit.
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