Cellular differences in ring glands of flesh fly pupae as a consequence of diapause programming.

The ultrastructure of the ring gland (corpus cardiacum (CC), prothoracic gland (PG) and corpus allatum (CA)) was examined in diapausing and nondiapausing flesh fly pupae. The diapause developmental state, which is environmentally regulated and coordinated by the brain-ring gland complex, is associated with differences in the ultrastructure of PG and CA cells but not in the CC. During diapause the PG and CA cells have extensive arrays of rough endoplasmic reticulum and spherical mitochondria. The PG cells also contain lipid droplets surrounded by an electron dense amorphous coat not seen in PG cells from nondiapausing pupae. In nondiapausing pupae, the PG and CA cells contain large amounts of ribosomes throughout the cytoplasm but very little rough endoplasmic reticulum and elongated mitochondria. The fact that ring glands from diapausing pupae readily incorporate (35)S-methioninc indicates that the gland is actively synthesizing proteins, thus the contrasts in ring gland ultrastructure are not due to cellular quiescence during diapause but reflect fundamental cellular and physiological differences between the diapause and nondiapause developmental program.

Contribution of renal medullary mitochondrial density to urinary concentrating ability in mammals.

In mammals, the length of the loops of Henle increases with increasing body size without a concomitant rise in urinary concentrating ability. Because mass-specific metabolic rate falls with increasing body mass, this study sought to determine the extent to which this decline in metabolic rate could explain the low urinary concentrating ability of large mammals with long loops of Henle. Mitochondrial ultrastructural parameters were measured in the medullary thick ascending limbs (mTALs) of a series of nine mammalian genera ranging in body mass from 0.011 kg (bats) to approximately 400 kg (horses). The volume of mitochondria as a percent of mTAL cellular volume declined with increasing body mass (Mb-0.056). Inner mitochondrial membrane area per volume of mitochondrion also declined with increasing body mass (Mb-0.034), as did basolateral membrane area per unit mTAL cellular volume (Mb-0.075). Thus, not only do mitochondria occupy more volume of mTAL cells of smaller mammals, but those mitochondria are also more densely packed with cristae. Inner mitochondrial membrane area per unit volume of mTAL cell cytoplasm scaled as Mb-0.092. The decline in inner mitochondrial membrane area and basolateral membrane area per volume of mTAL cell may explain at least in part the relationship between body mass and renal concentrating ability in mammals of different sizes.

Turtle urinary bladder: regulation of ion transport by dynamic changes in plasma membrane area.

Turtle urinary bladder possesses four ion transport processes: Na+ absorption, H+ secretion, and HCO3- secretion-Cl- absorption. Each transport process is performed by a specific epithelial cell type. Granular cells absorb Na+ but they are not sensitive to antidiuretic hormone (ADH), unlike toad bladder granular cells. alpha-Carbonic anhydrase-rich (CA) cells secrete H+ via an apical H+-adenosinetriphosphatase (ATPase). Under conditions of low CO2 tension, this active pump is contained in the limiting membranes of certain cytoplasmic vesicles. The vesicles fuse with the apical membrane, and H+ pumps are incorporated into that membrane, as physiological conditions demand increased H+ secretion. The stimulus for fusion of these vesicles with the apical membrane appears to be intracellular acidification. beta-CA cells secrete HCO3- and reabsorb Cl-, both processes driven by H+-ATPase in the basolateral membrane in series with an apical Cl- -HCO3- exchanger. Increased intracellular adenosine 3',5'-cyclic monophosphate concentration in beta-cells stimulates net HCO3- secretion and induces an electrogenic component of this flux by activating an apical Cl- channel. This activation accompanies the fusion of an intracellular tubulovesicular network with the apical membrane. The membrane of this network may contain Cl- channels.

Correlation between apical intramembrane particles and H+ secretion rates during CO2 stimulation in turtle bladder.

To correlate the prevalence of rod-shaped intramembrane particles (RSP) in the apical membranes of carbonic anhydrase-rich (CA) cells and the H+ transport rate in turtle urinary bladder, we carried out morphometric studies by means of scanning and freeze-fracture electron microscopy of the alpha and beta subpopulations of CA cells. Correlations were made between the apical membrane areas of alpha cells and H+ transport rate at 0 and 5% ambient CO2. Exposure to CO2 more than doubled the planar area of the luminal surface of alpha cells and increased the degree of folding (amplification) of the apical cell membrane from 2.8 +/- 0.3 to 3.8 +/- 0.3. The actual apical membrane area of alpha cells increased from 176 mm2 to 693 mm2 per 8 cm2 epithelial area. The RSP density also appeared to be increased by about 40%. The total CO2-induced increase in RSPs in position at the luminal surface was 5 fold while the increase in H+ transport was 9-fold. We conclude that stimulation of H+ transport by CO2 involves recruitment of RSP to the apical cell membrane of alpha-type CA cells and that RSPs are associated with active H+ transport. They may represent linear arrays of transmembrane components of H+ pumps.

A double-membrane model for urinary bicarbonate secretion.

To define the transport pathway for HCO-3 secretion (JHCO3) across the apical and basolateral membranes of turtle bladder, we examined the effects of cAMP, isobutylmethylxanthine (IBMX), the Cl- channel blocker 9-anthroic acid (9-AA), and the disulfonic stilbene DIDS (4,4'-diisothiocyanostilbene-2,2'-sulfonic acid) on the electroneutral and electrogenic components of JHCO3. Total JHCO3 was measured by pH stat titration of the mucosal compartment after Na+ absorption and H+ secretion were abolished by ouabain and a delta pH, respectively. Addition of cAMP or IBMX increased total JHCO3 and induced a short-circuit current (ISC), accounting for a large part of JHCO3; net Cl- absorption was reduced. Mucosal 9-AA inhibited the IBMX-induced electrogenic component of JHCO3, whereas mucosal DIDS inhibited the electroneutral component and acetazolamide reduced both. We suggest that HCO-3 is generated within the cell by a Na-independent primary active acid-base transport at the basolateral membrane (H+ extrusion into the serosal compartment). Cellular HCO-3 accumulation drives JHCO3 via a Cl-HCO3 exchanger at the luminal membrane. IBMX and cAMP activate a 9-AA-sensitive anion conductance parallel to the exchanger. The apparent reversal of the transport elements between the two cell membranes (compared with H+-secreting cells) led to an ultrastructural examination of the carbonic anhydrase-rich cells.

Alpha and beta types of carbonic anhydrase-rich cells in turtle bladder.

The carbonic anhydrase-rich (CA) cell population of the turtle urinary bladder, which is responsible for the secretion of H+ and probably of HCO-3, was studied by freeze-fracture and thin-section electron microscopy. The apical membrane of the major CA cell type (alpha type) was characterized by microplicae and by a coat of studs on its cytoplasmic side; on freeze-fracture, it contained a dense population of rod-shaped intra-membrane particles. When fixed at low CO2 tension, the apical membrane area of the alpha cell was reduced; its surface displayed microplicae as well as microvilli, and the apical cytoplasm contained many vesicles with rod-shaped particles and studs. The apical membrane of the other (beta type) CA cell was characterized by numerous individual microvilli without microplicae and by a relative absence of rod-shaped particles and studs. Instead, the beta cell contained studs and rod-shaped particles in its basolateral membrane. The ultrastructure and frequency of the beta CA cell were not affected by changes in CO2 tension. We suggest that the alpha cell is responsible for H+ secretion. The reversal of the polarity of the membrane elements in the beta cell and failure to respond to CO2 with amplification of its apical membrane are consistent with a role in HCO-3 secretion.

Role of membrane fusion in CO2 stimulation of proton secretion by turtle bladder.

The changes in cell structure produced during stimulation of proton secretion by CO2 in turtle bladder were examined using ultrastructural morphometric methods. One hour after CO2 addition, the area of the luminal membrane of the carbonic anhydrase-containing (CA) cell population was increased 2.5-fold and the volume percent of electron-lucent cytoplasmic vesicles in these CA cells was decreased by 61%. No changes were observed in the epithelial granular cells. These results suggest that during CO2 stimulation the vesicles fuse with the luminal membrane. CO2 stimulation of proton secretion is inhibited by the cytoskeleton-disrupting drugs colchicine and cytochalasin B and by 99% deuterium oxide as the Ringer solvent. Deuterium oxide also inhibits the decrease in cytoplasmic vesicles. Thus stimulation of proton secretion by turtle bladder CA cells depends to a large extent on vesicle fusion and the resultant increase in luminal surface area.

Ultrastructural characterization of cholesterol distribution in toad bladder using filipin.

The polyene antibiotic filipin was used to characterize the cholesterol distribution in the membranes of the toad bladder epithelium in freeze-fracture replicas. The apical membranes of granular and mitochondria-rich cells incorporate moderate amounts of filipin while the basolateral membranes of both cell types incorporate substantially greater amounts. Intracellular membranes, in general, take up very little filipin. The major exception to this is the granule membrane, which appears to be rich in cholesterol. An inverse correlation was found between the density of filipin-sterol complexes in the apical membrane and the incidence of granules in the cytoplasm. This suggests that fusion of granules with the apical membrane may be responsible for variation in the concentration of cholesterol in the apical membrane. Thirty minutes following vasopressin exposure, there is no consistent change in the cholesterol content of the apical membrane of granular cells as measured by the incidence of filipin-sterol complexes. The lack of change in the amount of membrane cholesterol indicates that the vasopressin-induced increase in transepithelial water permeability is not mediated by a change in cholesterol content of the apical membrane.

Evaluation by capacitance measurements of antidiuretic hormone induced membrane area changes in toad bladder.

A technique for estimating effective transepithelial capacitance in vitro was used to investigate changes in epithelial cell membrane area in response to antidiuretic hormone (ADH) exposure in toad bladder. The results indicate that transepithelial capacitance increases by about 30% within 30 min after serosal ADH addition and decreases with ADH removal. This capacitance change is not blocked by amiloride and occurs whether or not there is a transepithelial osmotic gradient. It is blocked by methohexital, a drug which specifically inhibits the hydro-osmotic response of toad bladder to ADH. We conclude that the hydro-osmotic response of toad bladder to ADH is accompanied by addition of membrane to the plasmalemma of epithelial cells. This new membrane may contain channels that are permeable to water. Stimulation of Na+ transport by ADH is not related to membrane area changes, but appears to reflect activation of Na+ channels already present in the cell membrane before ADH challenge.

Morphologic alterations in the rat medullary collecting duct following potassium depletion.

Freeze-fracture and thin-section electron microscopy and morphometry were used to characterize further the response of the rat medullary collecting duct to potassium depletion. In freeze-fracture replicas, principal cells and intercalated cells were identified based on the assumption that intercalated cells possess a high density of rod-shaped intramembrane particles in their luminal membranes. Potassium depletion caused an increase in the relative number of cells with a high density of rod-shaped particles from the control level of 22% to 31% after 2 weeks and to 36% after 4 weeks. The frequency of intercalated cells identified by thin-section criteria was, however, about 35% in controls and unchanged by potassium depletion. This suggests that intercalated cells can have two types of membrane morphology. In potassium depletion, all intercalated cells display a high density of rod-shaped particles in their luminal membranes. In addition, the luminal membrane area of intercalated cells increased more than threefold, and the density of their rod-shaped particles increased by 21%. These observations suggest that the intercalated cell and its rod-shaped particle may be involved with the potassium reabsorption that occurs in this nephron segment with potassium depletion.