IMMUNOHISTOCHEMICAL LOCALIZATION OF INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS IN NONNEURAL TISSUES, WITH SPECIAL REFERENCE TO EPITHELIA, THE REPRODUCTIVE-SYSTEM, AND MUSCULAR TISSUES
S. Nakanishi et al., IMMUNOHISTOCHEMICAL LOCALIZATION OF INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS IN NONNEURAL TISSUES, WITH SPECIAL REFERENCE TO EPITHELIA, THE REPRODUCTIVE-SYSTEM, AND MUSCULAR TISSUES, Cell and tissue research, 285(2), 1996, pp. 235-251
Although the pharmacological properties and distribution of inositol 1
,4,5-trisphosphate (IP3)-sensitive calcium stores vary considerably am
ong tissues, studies of its localization have been devoted mostly to t
he central nervous system. In this report we have analyzed the localiz
ation of IP3 receptors in diverse non-neural tissues of the mouse, usi
ng polyclonal antibodies raised against purified IP3 receptors through
immunoblotting and immunohistochemistry. These antibodies mainly reco
gnized type 1 IP3 receptors, although they also reacted with other typ
es of IP3 receptors. The receptors were localized in the apical surfac
e areas of highly polarized epithelia, such as the choroid plexus, ret
inal pigment epithelium, and columnar epithelium lining the interlobul
ar ducts in the sublingual and submaxillary salivary glands. Immunoele
ctron microscopy of choroidal cells revealed that IF3 receptors are lo
calized on the surfaces of several structures, including clear vesicle
s, tubules and vesicular profiles of smooth endoplasmic reticulum, rou
gh endoplasmic reticulum and a part of the nuclear envelope; as well a
s clusters of ribosomes in the cytoplasmic matrix. The surface areas o
f ciliated epithelia, such as those of the trachea and oviduct, also s
tained positive. The cytoplasmic distribution was homogeneous in mesan
gial cells, myoepithelial cells, and endothelial cells accompanying mu
scle, as well as in a population of endocrine cells. Intense immunosta
ining was found in the surface areas as well as in the cytoplasm of di
verse smooth muscle cells. Staining intensity of smooth muscle varied
among cells in the same tissue. Staining was intense in the cytoplasm
of premature oocytes in the primary follicle, but then attenuated as t
hese cells matured. The Sertoli cells with clusters of elongating matu
ring sperm were stained, but mature sperm were unstained. These result
s indicate a heterogeneous cellular distribution, and possibly a heter
ogeneous subcellular distribution, of a population of IF3 receptors in
a variety of non-neural tissues.