LOCALIZATION AND MOLECULAR HETEROGENEITY OF SULFATED GLYCOPROTEIN-2 (CLUSTERIN) AMONG VENTRAL PROSTATE, SEMINAL-VESICLE, TESTIS, AND EPIDIDYMIS OF RATS
Ja. Sensibar et al., LOCALIZATION AND MOLECULAR HETEROGENEITY OF SULFATED GLYCOPROTEIN-2 (CLUSTERIN) AMONG VENTRAL PROSTATE, SEMINAL-VESICLE, TESTIS, AND EPIDIDYMIS OF RATS, Biology of reproduction, 49(2), 1993, pp. 233-242
In the rat reproductive tract, sulfated glycoprotein 2 (SGP-2) is pres
ent in the ventral prostate, seminal vesicle, testis, and epididymis.
In the ventral prostate, SGP-2 is associated with the process of progr
ammed cell death, while in the testis and epididymis a role for SGP-2
in sperm maturation has been proposed. Available information suggests
that there are both inter- and intra-organ variations in SGP-2 localiz
ation, molecular forms, and response to androgen ablation. In the pres
ent study, localization of SGP-2 within the ventral prostate, seminal
vesicle, and epididymis was compared by immunohistochemistry. In the v
entral prostate of intact rats, immunoreactive SGP-2 was confined to a
discrete population of epithelial cells lining the proximal ducts. Ep
ithelial cells in other regions of the ventral prostate did not stain
for SGP-2. A similar staining pattern was observed for the seminal ves
icle; a small population of SGP-2-expressing epithelial cells was foun
d in epithelium that did not stain for SGP-2. The epididymis also demo
nstrated a non-uniform staining pattern. The caput displayed strong im
munoperoxidase reaction over the apical membrane and stereocilia of al
l principal cells. Principal cells also showed variable degrees of cyt
oplasmic staining ranging from weak to strongly positive. The corpus a
nd cauda showed a similar staining pattern. After castration, all epit
helial cells in the ventral prostate and seminal vesicle became intens
ely positive for SGP-2 staining. In the caput and cauda epididymis the
re was an increase in the number of principal cells demonstrating stro
ng intracellular staining for SGP-2. These results suggest that as obs
erved previously in the regressing ventral prostate, increased intrace
llular SGP-2 staining may also be associated with the regressing epidi
dymis and seminal vesicle. Differences in molecular forms of SGP-2 wer
e investigated by two-dimensional Western and lectin blots. Molecular
forms of SGP-2 differed between testis and epididymis but were similar
between ventral prostate and seminal vesicle. Prostate and seminal ve
sicle forms of SGP-2 differed from those of both testis and epididymis
. Analysis of terminal carbohydrate present on the various SGP-2 molec
ular forms also confirmed the existence of heterogeneity. These result
s demonstrate the presence of multiple molecular forms of SGP-2 in var
ious organs of the male reproductive tract in rats and suggest a possi
ble variation in functional activity and/or half-life of SGP-2 in thes
e organs.