Vol. 75, No. 2, 1977
BIOCHEMICAL
LTPO'IROPIN:
AND BIOPHYSICAL
LOCALIZATION
BY RADIOIMMUNOASSAY
OF ENDORPHIN PRECURSOR IN PITUITARY
Frank
LaBella2,
Department University
of Pharmacology and Therapeutics of Manitoba, Faculty of Medicine Winnipeg, Manitoba, Canada
Clinical
February
AND BRAIN1
Gary Queen and Jan Senyshyn
Martin
Received
RESEARCH COMMUNICATIONS
Lis
and Michel
Chretien
Research Institute of Montreal 110 avenue des Pins Ouest Montreal, Quebec, Canada
8,1977 SUMMARY
Beta-Lipotropic Hormone (LPH) was estimated in pituitary and brain by a radioimmunoassay specific for the N-terminal, non-opiate portion of the protein, and endorphin activity by an opiate radioreceptor assay. The intermediate pituitary is most concentrated in LPH and endorphin. Gel filtration indicated the presence in the pituitary of intact LPH and N-terminal fragments but only intact LPH in brain. Endorphin activity in pituitary is associated primarily with a component of 3000 daltons and to a lesser extent with one of about 2000 daltons. Brain endorphin activity is mostly accounted for by a 2000 dalton component, enkephalins representing an apparently minor activity. In pituitary and brain LPH and endorphin are entirely associated with a 12,000 g/10 min fraction. A family from
brain
N-terminal peptide
ization
(l-5).
pentapeptide
sequence
in
of paired
is
found
0 I977
active
in several contained
by the Medical of the MRC
by Academic
of reproduction
in any
Research
Press, Inc.
form
reserved.
within Council
(endorphins)
share
members
in
acid
vary
residue
cells
a common
length.
(6-9).
Thus,
LPH and the and NMUD/Health
The beta-
The localsuggests
points
of this
structure
and the major (10).
isolated
protein,
gland
A protein
the prohormone
contained
has been
in the LPH sequence
fragments.
endocrine
actions
pituitary
residues
peptide
within
peptide
a 91-amino in the
acid
other
peptides
and individual
within
amino
morphine-like
These
identified
basic
one hormonal
1 Supported 'Associate
contained (LPH)
yielding
each case is
sents
Copyright All rights
is
Hormone
of cleavage type
with
and pituitary
sequence
Lipotropic
of peptides
hormone
structure
beta-MSH
repre-
endorphin
sequence,
and Welfare
Canada
350 ISSN
0006-291X
Vol. 75, No. 2, 1977
another. tered
BIOCHEMICAL
In analogy within
with
a secretory
and active
peptide
associated
with
pituitary.
the granules.
chymal
cells
is
work
one would
consisting
of the
our
granules all
expect
of prohormone,
obtained
endorphin
intermediate
of granules
laboratory
of the activity
Pituitary
the distribution
lobe
in brain
in
fraction
pituitary
is
remains
LPH to be sequescleaving
endorphin
enzyme(s)
activity
from homogenates tissues
apparently pituitary
is
derived gland,
pituitary
that
was
of brain
and
contained from
whereas
to be determined.
LPH parallels
the intermediate
from
(11,12)
in these
of the
of immunoreactive
most concentrated
same granule
from
cytoplasmic
within
that
package
Essentially
source
hormones,
fragments.
In previous
cellular
other
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
parenthe
We now show of endorphin;
and associated
with
it the
or brain.
EXPERIMENTAL Antibodies to ovine beta-LPH were developed in rabbits against the hormone conjugated to ovalbumin with carbodiimide. The ratio of LPH to ovalbumin in the conjugate was 1O:l. (We are grateful to Dr. P. Schiller for preparation of the conjugate). Three days before immunization animals were injected subcutaneously with 0.5 ml of crude Bordella pertussis vaccine. The first immunization was carried out with 500 ug LPH in complete Freund's adjuvant intradermally, and a booster given at six weeks. A second injection contained 250 us LPH in incomplete adjuvant. Methionine5,enkephalin (LPI-I 6165) and leucine enkephalin were obtained from Peninsula Laboratories, San Carlos, CA, and alpha-endorphin (LPH 61-76) from Dr. R. Guillemin. Bovine pituitary glands and brains were obtained from freshly killed cattle of unspecified age and sex and transported on ice to the laboratory. About 2 hr elapsed between death of the animal and extraction of tissue. For estimation of LPH, 10% homogenates of tissues in ice cold water were extracted with a final concentration of 2 M acetic acid and serial dilutions of the extracts made in 0.05 M TRIS buffer, pH 7.4. Dilutions of tissue extracts were assayed by solid phase radioimmunoassay, as previously described for other pituitary For gel filtration the 480,000 g-min fraction, containing hormones (13). essentially all the tissue LPH from 0.5 - 1.0 g tissue was extracted in 10 volumes of 2 N acetic acid, freeze-dried, and the residue in 1 ml of 2 N acetic acid was applied to the column. The sample was eluted with 2 N acetic collected. Column acid, with a flow rate of 0.2 ml/min and 0.5 ml fractions dimensions: G-15 and G-50, 1 x 47 cm, and G-25, 1.5 x 66 cm. Endorphin activity was estimated by a radioreceptor assay with 3H-naloxone as previously Centrifugation pellets were suspended in 2 N acetic acid, described (11,12). stirred at room temperature for 30 min, centrifuged, and the supernatant assayed. RESULTS AND DISCUSSION A schematic sequences
between
of the LPH molecule
paired
basic
amino
acid
351
is
shown in Figure
residues
indicated.
1, with
the
The LPH anti-
Vol. 75, No. 2, 1977
BIOCHEMICAL
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
. NH1
i
I
39 41
1 1 1
-
0 COOH 91
58 61
RADIOIMMUNO 39
ASSAY 58 91 OPIATE 61-65 61-76 61
ASSAY
91
FIGURE 1. Schematic of ovine LPH showing location of known and the fragments determined by radioimmunoassay and opiate assay.
peptide products radioreceptor
CPM 9500-
6500-
3500.
0.001
0.01
0.1
10
1.0
100
us/ml
FIGURE 2. Activity radioimmunoassay.
serum
appears
polypeptide does
to
the
intact
sequence
leucine active
be
(Figure
cross-reactivity,
only
of LPH (l-91)
2).
LPH molecule.
The opiate-like
the assay.
Beta-MSH antigenic
(gamma-LPI0 (residues
C-terminal
reacts 41-58)
fragment
Methionine (residues
purified
bovine
352
in
the solid-phase
the N-terminal
determinants
and alpha-endorphin Several
fragments
against
1-58
0.1% cross-reactivity.
enkephalin in
primarily
Sequence
indicating
l-40.
about
directed
and peptide
almost shows
of the
as well very
as
low
to reside
within
the
(residues
61-91)
shows
enkephalin 61-76) anterior
portion
(residues are
61-65),
completely
pituitary
in-
hormones
Vol.
75,
No.
1977
2,
BIOCHEMICAL
mg
AND
Tissue
BIOPHYSICAL
Equiv.
(Wet
0.1
RESEARCH
COMMUNICATIONS
Wt.)
1.0
10 ng LPH/mg INT.
PIT.
690
POST. ANT.
PIT. PIT.
150
CAUDATE
10
I
I
30
100
ng
LPH
FIGURE 3. Dose-response curves brain in the LPH radioimmunoassay.
(NIAMD-USPHS) for
cross-react
LPH estimates
on the other for
the
hand,
sequences
is
tissue
(Figure
As shown
is
intact
3).
concentrated
than
be very
in endorphin.
observed
and these
permits
tissue.
It
products
differs
assessment
can be seen between
curves
by the
brain
(RIA) assay,
and sizes the
and pituitary.
353
pituitary
gland
the assay
for
intermediate Brain
LPH lobe
is much less known to
nucleus
in LPH levels
are
elsewhere.
of the types 4) that
caudate
differences
be presented
the
in LPH.
with
brain
and
of LPH, specifically
in
(11,121
in conjunction
(Figure
The opiate
region
concentrated
Regional will
lobes
the radioimmunoassay
of the bovine
endorphin
as represented
findings
Gel filtration, assay,
least
pituitary,
lobes
dose-response for
lobe
Thus,
pituitary
61. three
show parallel previously
0.1%.
the C-terminal
residue of the
of bovine
and the N-fragment.
for
with
most and the anterior
rich
than
protein
selective
of each
and of brain
of extracts
to less
beginning
Extracts
103 3
the RIA and opiate of LPH fragments
profile
of LPH and its
In the
pituitary,
radioreceptor in a given cleavage intact
LPH
Vol.
75,
No.
2,
1977
BIOCHEMICAL
AND
BIOPHYSICAL
RESEARCH
LPH
Endorphin
h/ml)
(nM
I
Cytochrome
0
Vitamin
from
the G-25
daltons) gel.
is
Volume
antiserum
may represent
endorphin
component,
fragment.
A minor
components
approaching
The position In brain,
about endorphin the
intact
)
(ml )
of bovine is shown
by the
components
fragments
of synthetic only
indicated
Smaller
Equiv.
812
FIGURE 4. Gel filtration of extracts and of brain. LPH in column fractions activity in the right panels.
10,000
Noloxone
C
Elution
(about
COMMUNICATIONS
3,000
size
of enkephalin
enkephalin
LPH (l-91)
daltons
354
excluded directed
The major
corresponds
to the 61-91
can be identified,
are detectable
was determined is detectable
N-terminal
respectively.
probably
2,000
of a component
by the
and l-39,
daltons,
of about
presence
detected
1-58
neuro-intermediate pituitary in the left and endorphin
on each
by RIA,
in
but
pituitary.
of the columns.
indicating
that
N-
no
BIOCHEMICAL
Vol. 75, No. 2, 1977
LPH (% of total
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
I
-kpiT. kE i:/r:;lT.p’T. /~ANT.p 3
12 48
3
s g-min
FIGURE 5. Distribution pituitary lobes.
terminal
fragments
C-terminal 2,000
daltons.
small
proportion
of LPH among subcellular
are degraded
opiate
fragments
or removed
Enkephalin
activity
(Figure
derived
peptide
products
sedimentation (11,121.
are
forces
of 12,000
elaborating lipolytic
peptide activity
pituitary
and
of about
in a relatively
show LPH to be most concentrated We showed
and brain stored
the
within 5) is
g or less.
and endorphin
product
packaging
hormones (17,181
is
(10). this
amino
Although
biological
355
putative
endorphin,
acid
to that
is
the
The
of endorphin compo-
sedimented
at
in LPH and the protein
in several
is
and its
granule.
LPH has been shown property
lobe
in particulate
residues within
pre-
intermediate
to that found
in
prohormone
granules
structures
analogous
in the
identical
of LPI-I-containing The paired
that
the same secretory
of the LPH activity
proportion
of beta-i%H secretion
brain
generation.
component
apparently
most concentrated
of LPH (Figure all
and the great
present
from
their
by a major
(14-16).
also
apparently
pattern
nents,
suggest
pituitary
in
Essentially
recognition
studies
from LPH, is
Furthermore,
(11,12).
is
fractions
4).
of the intermediate
sumably
s
soon after
are represented
Immunohistochemical cells
12 48
x 10 4
sequence other
glands
to possess
not impressive
and,
Vol. 75, No. 2, 1977
until
recently,
enigmatic. is
physiological and his
synthesized
thus
were
done before
In the
present
to be the 61-91
artifacts
of extensively we find
of about
the
2,000
(residues
61-76).
accounted
for
ponent
(about
by Hughes
(1)
LPH-endorphin
components
processed
tissue
component
to predominate,
consistently
61-911,
l-39), are
In contrast,
and two endorphin
of fresh
61-91)
beef
found
upon demand,
(201,
is
last of
only
within
smaller
products
is
another
identified a minor
component.
peptide
The endocrine
products,
i.e.
and beta-endorphin
apparently
yield
the major
granule
in
intact
those
the
LPH only,
opiate
component
may be mobilized from
com-
in brain
a systemic
storage
distinct
activity
daltons;
41-58),
LPH in brain
component
alpha-endorphin
the
than
pituitary
a minor
endorphin
2,000
gland
representing
bovine
although
represents
(residues
in pituitary. to yield
In fresh
the pentapeptide
of brain
both
these
pituitary
apparently
brain
of about
present
extracts
l-58
and the release
in the
as each of the major
apparently
that
to fragment
However,
presumably
presumably
beta-MSH
components,
(4,5).
present,
and Snyder
(residues
synapses
smaller
and Simantov
N-fragment
(residues
fragment,
LPH, as well
rise
of endorphin
endorphin
in pituitary
to propose
(unpublished).
presumably
Intact
pituitary.
fragment.
500 daltons),
secretion.
(residues
the C-terminus
the major
is
has been
the first
and gives
by the component
complex
were
protein
pituitaries
recently
In extracts
chiefly
(9)
studies
61-91
daltons
of the
the discovery
until
appears
glands
colleagues
releasing
was not verified
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
significance
in bovine
presumably
experiments 61-91
the Chretien
beta-LPH (19),
BIOCHEMICAL
at
in pituitary.
REFERENCES 1. 2. 3. 4. 5.
Hughes, .I., Smith, T.W., Kosterlitz, H.W., Fothergill, B.A. and Morris, H.R. (1975). Nature, 258, 577-579. Guillemin, R., Ling, N. and Burgus, R. (1976). C.R. ser. D., 282, 783-785. Bradbury, A.F., Smith, D.G. and Snell, C.R. (1976). Res. Commun., 69, 950-956. Cox, B.M., Goldstein, A. and Li, C.H. (1976). Proc. 73, 1821-1823. Goldstein, A. (1976). Science, 193, 1081-1086.
356
L.A., Acad.
Morgan, Sci.
Biochem. Natl.
(Paris) Biophys.
Acad.
Sci.,
Vol. 75, No. 2, 1977
6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20.
BIOCHEMICAL
AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Graf, L. and Li, C.H. (1973). Biochem. Biophys. Res. Commun., 53, 1304-1309. Li, C.H., Barnafi, L., Chretien, M. and Chung, D. (1965). Nature, 208, 1093-1094. Gilardeau, C. and Chretien, M. (1970). Can. J. Biochem., 48, 1017-1021. Chretien, M. and Gilardeau, C. (1970). Can. J. Biochem., 48, 511-516. Polypeptide Hormones: Molecular and Cellular Aspects, Ciba Found. Elsevier, New York (1976). Syw., Queen, G., Pinsky, C. and LaBella, F. (1976). Biochem. Biophys. Res. Commun., 72, 1021-1027. LaBella, F., Queen, G. and Pinsky, C. (in press). Canad. J. Physiol. Pharmacol. LaBella, F,, Dular, R., Queen, G. and Vivian, S. (1975). Endocrinology, 96, 1559-1565. Moon, H.D., Li, C.H. and Jennings, B. (1973). Anat. Rec., 175, 529-538. nessy, C., Herlant, M. and Chretien, M. (1973). C.R. Acad. Sci. (Paris) 338, 276-335. Furth, J., Chretien, M., Moy, P. and Granman, J. (1975). Amer. J. Pathol., 78, 20. Birk, Y. and Li, C.H. (1964). J. Biol. Chem., 239, 1048-1052. Lie., M., Gilardeau, C. and Chretien, M. (1972). Acta Endocrinol., 69, 507-510. Chretien, M., Lis, M., Gilardeau, C. and Benjannet, S. (1976). Can. J. Biochem., 54, 566-570. Simantov, R. and Snyder, S.H. (1976). Proc. Natl. Acad. Sci., 73, 2525-2519.
357