Changes in chloride cell distribution during early larval stages of Clupea harengus

A non-uniform distribution of cutaneous chloride cells was found in the early, pre-feeding larval stages of herring Clupea harengus . Chloride cells on the head, yolk-sac and trunk regions were unevenly distributed, whereas more densely packed chloride cells were observed in the pericardial and prebranchial regions. The pattern of chloride cell distribution changed during development and two distinct changes are described. The density of choride cells on the ventral trunk increased substantially during the period of yolk absorption, presumably due to contraction of the yolk sac and selective retention of yolk-sac chloride cells. Also during this period the cells on the lateral body wall increased in number and became distributed in segmental bands overlying the myosepta. Most chloride cells were found in association with the haemocoel or primordial blood vessels. Superficial segmental blood vessels were not found in the early larva, but the segmental bands of chloride cells overlay nerve tracts in the myosepta which were tentatively identified as the focal innervation of myotomes. It is concluded that both the circulatory system and the peripheral nervous system may play a role in determining chloride cell distribution in early larvae.     

Ultrastructural features of chloride cells in the gill epithelium of the Atlantic salmon, Salmo salar, and their modifications during smoltification

To elucidate the ultrastructural modifications of the gill epithelium during smoltification, gills of the Atlantic salmon (Salmo salar) were examined by electron microscopy at three stages of this process, which were defined as follows: "parrs" were freshwater fish that had not yet started their transformation; "freshwater smolts" were freshwater fish that were ready to enter seawater; and "seawater smolts" were smolts that had been transferred from fresh water and maintained for 4 days in seawater (35%). In the gill epithelium of parrs, there were two types of chloride cells. The large chloride cells contained deeply stained mitochondria and numerous apical, irregular, dense, membrane-bound bodies that formed 77% of the chloride cell population and were distinguished easily from small chloride cells that have distinctly paler mitochondria and no dense bodies in their apical cytoplasm. In freshwater smolts, the large chloride cells formed 95% of the chloride-cell population. In contrast to the small chloride cells that were not modified, they almost doubled in size. Their tubular system developed extensively to form a tight network with regular meshes significantly smaller than those observed in parr chloride cells. Forty percent of the large chloride cells were associated with a new type of cell, the accessory cell, to which they were bound by shallow apical junctions. Half of these accessory cells were not seen to be in contact with the external medium. In seawater smolts, 80% of the large chloride cells were associated with accessory cells. Most accessory cells reached the external medium and sent numerous cytoplasmic interdigitations within the apical portion of the adjacent chloride cells. As a result, a section through the apical portion of the chloride cells and their associated accessory cells revealed a mosaic of interlocked cell processes bound together by an extended, shallow apical junction. It was concluded that the Atlantic salmon develops in fresh water most of the ultrastructural modifications of the gill epithelium which in most euryhaline fish are triggered by exposure to seawater. The effective transfer into seawater would act only as a final stimulus to achieve some adequacy between the freshwater smolt and its new environment.     

Ultrastructural features of mitochondria-rich cells in stenohaline freshwater and seawater fishes

In order to elucidate the functional significance of accessory cells in freshwater fishes, such as the rainbow trout, which displays a poor adaptability to seawater life, a search for such cells was performed in two stenohaline freshwater fishes: the loach and the gudgeon. Accessory cells were never encountered in these species; but, in contrast, two types of chloride cells were observed consistently that strikingly resembled the alpha- and beta-cells previously described in the guppy, a freshwater-adapted euryhaline fish. The alpha-cell, a pale and elongated chloride cell, was located at the base of the secondary lamellae in close contact with the arterioarterial pillar capillary. Darker, ovoid chloride cells resembling the beta-cell were found exclusively in the interlamellar region of the primary epithelium facing the central venous sinous. The latter cells frequently formed multicellular complexes linked together by deep, narrow, apical junctions. In another experiment, a stenohaline seawater fish, the turbot, was adapted to diluted 5% saltwater and to fresh water. In seawater, the gill epithelium contained only one type of chloride cell, always associated with accessory cells. Due to numerous cytoplasmic interdigitations between the accessory cells and the apical portion of the chloride cell, there was a noticeable increase in the length of the shallow apical junction, sealing off the intercellular space between the two cell types. In 5% saltwater, there was a decrease in the number of these interdigitations and a concomitant decrease in the length of the shallow apical junction. In fresh water, chloride cells were partially or completely separated from the outside medium by modified accessory cells. It is thus concluded that accessory cells are found exclusively in fish living in seawater or preadapted to seawater and that they probably are involved in the formation and modulation of paracellular pathways for ionic excretion. In contrast, the respective roles of the two types of chloride cells observed in freshwater fishes are still to be determined.     

Fine structure of chloride cells in freshwater- and seawater-adapted Oreochromis niloticus (Linnaeus) and Oreochromis mossambicus (Peters)

Ultrastructural features of branchial chloride cells in Oreochromis niloticus (Linnaeus) and O. mossambicus (Peters) adapted to both fresh water and sea water were compdred. In freshwater adapted fish of both species chloride cells showed similar morphological features. Multicellular complexes made of a mature chloride cell and one or more accessory cells sharing a single apical crypt have been observed. Whereas high percentages of 0. mossambicus survived at maximum salinity only a few individuals of 0. niloticus showed the capacity to adapt to sea water. In the seawater-adapted individuals of 0. niloficus and 0. rnossambicus the chloride cells showed a two- and three-fold increase in sizei. respectively. Most chloride cells are organized in large multi-cellular complcxcs with apical interdigitations of accessory cells and 'leaky junctions'. These results indicate that the difference in euryhalinity of the species studied is related to functional rather than structural differences.     

Corn Mitochondrial Swelling and Contraction-an Alternate Interpretation

Mitochondria isolated from 3-day-old etiolated corn shoots (Zea mays L.) can be categorized into three separate groups, each group characteristic of the cell type from which the mitochondria were isolated. Phloem sieve tubes and some adjacent parenchyma cells contain mitochondria that have few cristae and little amorphous matrix. Mitochondria from meristematic and undifferentiated cells have more cristae and matrix. Vaculate and differentiated cells have mitochondria with well-developed cristae and abundant matrix. Each mitochondrial type exhibits typical in vitro spontaneous swelling and substrate-induced contraction responses. characterized by change or lack of change in cristae size and in density of amorphous material. For the second and third types of mitochondria, swelling and contraction are characterized by a change in degree of cristae size and in matrix density. The first type undergoes few changes upon swelling or contraction. Radical changes of the inner membrane, withdrawal and infolding, are associated with cell differentiation and not with swelling and contraction of isolated corn shoot mitochondria.     

Hyperplastic processes in cardiac muscle mitochondria exposed to toxic doses of adrenaline]

Experiments were conducted on albino rats; a study was made of hyperplastic processes in the mitochondria of the myocytes of the heart with the action of toxic adrenaline doses. A solution of adrenaline chloride was injested intramuscularly (3 mg/kg). Three types of mitochondria were revealed in electron microscopic study. Mitochondria of the first type were of the size and structure characteristic of the muscle cells of the myocardium. Mitochondria of the second type had a very dense, finegrained matrix and a great number of cristae per unit of the area. Mitochondria of the third type had two "sections" under the common external membrane, differing from one another by the matrix density, distribution and number of cristae. It is supposed that the ultrastructural peculiarities of each of the types reflected their functional condition.     

Identification of respiratory and ion-transporting epithelia in the phyllosoma larvae of the slipper lobster Scyllarus arctus

Phyllosoma larvae of the Palinura lack a branchial cavity and gills. In the phyllosoma, gas and ion exchanges that occur at the level of the gill in the adult must occur in other parts of the body or through the entire body. The objective of this study was to localize epithelia bordering the body of the phyllosoma larvae that had features comparable to those of the gill epithelia of adult decapods. The first phyllosoma instar of the small Mediterranean slipper lobster Scyllarus arctus was studied. First, we used a silver nitrate staining method to identify parts of the body with high ionic permeability. Confocal laser scanning microscopy with a fluorescent vital stain for mitochondria, dimethylaminostyrylmethylpyridiniumiodine (DASPMI), was then used to localize cells with a high density of mitochondria. Next, an ultrastructural study of selected epithelia was carried out. A thick (5 microns) mitochondria-rich epithelium covers the ventral side of the cephalic shield; its cells are characterized by the presence of well-developed apical infoldings adjacent to the cuticle. This part of the body has a high ionic permeability as indicated by a positive silver nitrate staining. The ventral mitochondria-rich epithelium might be involved in active ion transport. The rest of the body, particularly the dorsal side of the shield and the appendages, shows a lower ionic permeability (no positive silver nitrate staining) and is limited by a thin (1 micron) epithelium with low numbers of mitochondria. This epithelium exhibits features of a typical respiratory epithelium.     

Variations in mitochondrial size and ultrastructure during germ cell development

Summary Size variations and ultrastructural changes in mitochondria of developing germ cells of the female hamster were analyzed. Mitochondria in oogonia of foetus and newborn were elongate with transverse cristae. During pre-dictyate meiotic prophase they became small, rounded, and electron-dense with pleomorphic cristae. These changes were largely reversed when dictyate was reached. Maximum mitochondrial size and complexity of cristae were reached just at the beginning of the phase of rapid oocyte growth, and thereafter declined. As mitochondrial size and number of cristae decreased in the rapidly enlarging oocyte, the ratio of length to width increased, as did electron density of the matrix, until the formation of an antrum within the follicle. After antrum formation, the mitochondria again became more rounded and cristae were seldom seen. An attempt is made to correlate changes of mitochondrial morphology with other events occurring during oogenesis.The author wishes to thank the Department of Anatomy, University of Dundee, for financial support and for the use of the AEI EM 801 electron microscope     

Angle Meristem Origin and Development in Selaginella martensii

The origin and early development of angle meristems (AMs) inSelaginella martensii were studied using a high-resolution mouldand cast technique for scanning electron microscopy, in conjunctionwith light microscopy. Both dorsal and ventral AMs originatein the apical region shortly after the most recent bifurcationof the shoot apex. AMs appear to arise from a single superficialinitial cell, which subsequently undergoes an oblique anticlinaldivision to establish the apical cell of the AM. The AM apicalcell has a relatively short active life and divides laterallyusually only six to twelve times; most cells of the AM originatefrom repeated divisions of apical cell derivatives. Dorsal andventral AMs show similar developmental sequences, although theydiffer slightly in time of appearance. Ventral AMs originatedfirst, dorsal AMs appearing shortly thereafter. At a given branchpoint, the ventral AM is typically larger than the correspondingdorsal AM. Both dorsal and ventral AMs grow out as rhizophores(aerial roots), although ventral AM development greatly precedesdorsal AM development. It is possible that the apparent earlierdecrease in apical cell activity in dorsal AMs compared to ventralAMs could account for the lag in dorsal AM development as arhizophore at a given branch point. Selaginella martensii Spring, Lycophyta, angle meristem, apical cell, morphogenesis, mould and cast technique, replica technique, scanning electron microscopy     

Ejaculatory duct of the migratory grasshopper,Melanoplus sanguinipes (fabr.) (Orthoptera : Acrididae): A histological and ultrastructural analysis

The ejaculatory duct of the migratory grasshopper (Melanoplus sanguinipes [Fabr.]) (Orthoptera : Acrididae) is divisible into 3 regions: upper ejaculatory duct (UED) into whose anterior end the accessory glands and vasa deferentia empty; the funnel characterized by its slit-like lumen; and the lower ejaculatory duct (LED). Anteriorly, the UED has a keyhole-shaped lumen surrounded by a thin intima and highly columnar epithelial cells whose most conspicuous feature is massive aggregations of microtubules. More posteriorly, the UED lumen differentiates into dorsal and ventral chambers, the former having a thick cuticular lining armed with spines. In the hindmost part of the UED, the ventral chamber expands to obliterate the dorsal chamber; its cuticular lining thickens, and conspicuous lateral evaginations develop. The thick cuticle includes 3 distinct layers and on its surface carries numerous spatulate processes. In this region, the epithelial cells develop numerous short microvilli beneath which are many mitochondria. As the funnel is reached, the intima becomes extremely thick, and the epithelial cells lack microvilli and most microtubules. Within the funnel, a new, very distinct form of cuticle appears, which is in “units”, each associated with an epithelial cell and having a rounded epicuticular cap. The new cuticle arises ventrally but rapidly spreads to encircle the entire lumen, at which point the LED is considered to begin. Beneath this new cuticle, the epithelial cells are columnar, have long microvilli, numerous mitochondria in the apical cytoplasm, and rough endoplasmic reticulum basally. Apically, adjacent cells are tightly apposed; however, prominent intercellular channels develop more basally. The ejaculatory duct's features are briefly discussed in terms of its role in spermatophore formation.     

Ultrastructural features of the ventral prostate epithelial cells in the Australian plains rat, Pseudomys australis

The fine structure of epithelial cells of the small ventral prostate of Pseudomys australis males was studied. The cells were sometimes binucleated, exhibited relatively little granular endoplasmic reticulum, generally few secretory granules (probably reflecting a low proteinaceous secretory activity), but had abundant agranular endoplasmic reticulum (AER), similar to that in steroidogenic cells. Some of the mitochondria also showed tubular cristae. Furthermore, most cells had some irregular dense bodies in the cytoplasm which may have developed, by a gradual transformation process, from the membranes of AER, mitochondria and other organelles; they could be the product of degenerative changes in these organelles. These findings indicate a significant difference in the structure of these cells from those present in the ventral prostate of the hopping mouse, Notomys alexis. It is speculated that this gland secretes relatively little protein but perhaps more lipid or cholesterol-derived substance.     

Occurrence and Ultrastructure of Collar Cells in the Stomach Gastrodermis of Polypodium hydriforme Ussov (Cnidaria)

The existence of collar cells lining the stomach gastrodermis in free-living Polypodium hydriforme and their ultrastructure are described. The collar cells are provided with a collar consisting of 9–10 microvilli which encircles a central flagellum and forms a flagellar pit. At the bottom of the pit around the basal part of the flagellum there is fine crystalline material which extends also in the spaces between the microvilli and keeps them straight. The flagellum has a typical axoneme (9+2), its basal body is located below the apical surface of the collar cell and continues into a striated rootlet. An accessory centriole is situated close to the upper part of the rootlet. The cell nucleus is located in the basal part of the cell. Prominent mitochondria with tubular cristae, Golgi cisternae and fragments of rough endoplasmic reticulum are situated mostly in the basal part of the cytoplasm. Discoidal vesicles are abundant in the apical cytoplasm. The collar cells are connected to each other by septate junctions and interdigitations. The ultrastructure of collar cells described here is discussed in comparison to that of other Cnidarians and in connection with the problem of Polypodium's systematic position.     

Ultrastructure and immunocytochemistry of the nervous system of the larvae ofLingula anatina andGlottidia sp. (Brachiopoda)

Summary Planktotrophic brachiopod larvae ofGlottidia sp. have been investigated for the occurrence of glyoxylic acid induced fluorescence in catecholamines (CA), and serotonin-like (5-HT) and neuropeptide FMRFamidelike (FMRFamide) immunoreactivity (ir). The location of CA, 5-HT-ir and FMRFamide-ir cells and processes were compared with the location of neurons and nerve processes found by transmission electron microscopy. The apical ganglion contains 5-HT-ir and FMRFamideir cells and processes and CA processes. From the dorsal part of the apical ganglion extend dorsal 5-HT-ir and FMRFamide-ir processes; from the nine pairs of tentacles stage (9. pt) they project to the ventral ganglion. These dorsal lophophore processes follow themusculus lophophoralis and them. brachialis. The 5-HT-ir and some of the FMRFamide-ir processes project along the muscles to the tentacles. From the ventral part of the apical ganglion extend CA, 5-HT-ir and FMRFamide-ir processes which follow the ciliary band of the lophophore and project to the tentacles. An intense band of CA processes was also observed in the lophophore, but the dorsal/ventral location could not be ascertained. The ventral ganglion contains 5-HT-ir and FMRFamide-ir cells which project either caudally on the metasome or rostrally as part of the dorsal lophophore processes. The neuropil of the ventral ganglion contains CA, 5-HT-ir and FMRFamide-ir processes. The nervous system of the planktotrophic brachiopod larvae seems to consist of a ventral lophophore system innervating the ciliary bands and a dorsal lophophore system including the ventral ganglion innervating the body musculature. The latter system develops later in ontogeny and is regarded as a specialization due to the presence of shells and associated musculature. The former system is regarded as homologous with the nervous system of actinotroch larvae (Phoronida) and planktotrophic larvae of the echinoderms.     

Giant mitochondria distinct from enlarged mitochondria in secretory and ciliated cells of gerbil trachea and bronchioles

Numerous mitochondria ranging from slightly larger than normal to several micrometers in diameter (giant) were found in about one-half the serous secretory cells in the surface epithelium of the normal gerbil trachea and proximal bronchi. Tracheal serous cells of mice also were found to contain numerous giant mitochondria. Clara cells of gerbil bronchioles contained abundant giant mitochondria in addition to normal tubular mitochondria and the second population of enlarged spherical mitochondria that have been described in Clara cells of several genera. In contrast, mouse Clara cells revealed the normal tubular and the enlarged spherical mitochondria but no giant mitochondria. A survey of a number of cell types in gerbils failed to disclose hypertrophied mitochondria outside tracheobronchial surface epithelium and bronchioles. The mitochondrial enlargement resulted from an increase of matrix but not cristae. The expansion of matrix displaced the relatively sparse cristae into small collections compressed against the outer membrane. The prevalence of giant mitochondria and of granular endoplasmic reticulum is similar among cells, and these two organelles are codistributed within cells. The megamitochondria and granular reticulum occupy a central stratum, whereas normal mitochondria occur in the apical and basal regions. The giant mitochondria are considered related to a normal biologic activity that is characteristic of respiratory tract epithelium of mice and gerbils selectively and is more prominent in secretory cells than in ciliated cells.     

Two new species of Austrobdella (Hirudinida: Piscicolidae) from Chile

Austrobdella coliumicus n. sp. is described from Coliumo Bay, Chile. It is characterized by a continuous, external coelomic canal (= marginal lacuna), 5 pairs of testisacs, accessory gland cells, a body not distinctly divided into trachelosome and urosome, 2 pairs of dorsal ocelli on the trachelosome, dorsal and ventral segmental ocelli present on the urosome, green overall pigmentation with transverse brown bands, and the absence of conducting tissue. Austrobdella coliumicus is distinguished from other species of Austrobdella by the presence of 2 pairs of ocelli on the trachelosome and a more cylindrical body. It is unusual that this leech was collected from inside the mantle cavity of the razor clam, Ensis macha. Austrobdella losmoliniensis n. sp. is described from the electric ray, Discopyge tschudii, collected at Los Molinos, Chile. It is characterized by a continuous, external coelomic canal; 5 pairs of testisacs; accessory gland cells; a body distinctly divided into trachelosome and urosome; 1 pair of eyes on the oral sucker; overall black pigmentation with unpigmented areas; and the absence of conducting tissue. Austrobdella losmoliniensis can be distinguished from other species of Austrobdella by the combination of 1 pair of eyes on the oral sucker and black pigmentation.     

Ultrastructure of chloride cells in young adults of the anadromous sea lamprey, Petromyzon marinus L., in fresh water and during adaptation to sea water.

The chloride cells in the interlamellar areas of the gills of young adult, anadromous sea lampreys, Petromyzon marinus L., captured in fresh water undergo structural modification during the adaptation of these animals to sea water. In fresh water the chloride cells are partially overlapped by mucus-secreting superficial cells and contain an extensive reticulum of cytoplasmic tubules, which are confluent with both lateral and basal plasma membranes, numerous mitochondria, a Golgi complex of moderate size, and numerous apical vesicles. Adaptation to sea water results in a retraction of the superficial cells, exposing the entire apical surface of the chloride cells, and a proliferation of both cytoplasmic tubules and mitochondria. Extensive enlargement of the Golgi complex in the chloride cells of these animals suggests the involvement of this organelle in the proliferation of cytoplasmic tubules. The extracellular tracer, ruthenium red, enters the tubules from the lateral or basal intercellular spaces in both freshwater- and seawater-adapted animals but never enters either tubules or vesicles from the apical surfaces, indicating that these are not confluent. The presence of dividing basal cells and newly-forming chloride cells, combined with evidence of degeneration of chloride cells, suggests that there is a turnover of this cell type. Both superficial and basal cells are phagocytic and involved in heterophagy of degenerating chloride cells. This phenomenon occurs in both fresh water and sea water indicating that the chloride cells may be functional in both environments.     

Ultrastructure and cytochemistry of salivary glands of the predator Podisus nigrispinus (Hemiptera: Pentatomidae)

Podisus nigrispinus Dallas (Hemiptera: Pentatomidae) is a zoophytophagous insect with a potential for use as a biological control agent in agriculture because nymphs and adults actively prey on various insects by inserting mouthparts and regurgitating the contents of the salivary glands inside the prey, causing rapid paralysis and death. However, the substances found in saliva of P. nigrispinus that causes the death of the prey are unknown. As a first step to identify the component of the saliva of P. nigrispinus, this study evaluated the ultrastructure and cytochemistry of the salivary glands of P. nigrispinus. The salivary system of P. nigrispinus has a pair of principal salivary glands, which are bilobed with a short anterior lobe and a long posterior lobe, and a pair of tubular accessory glands. The principal gland epithelium is composed of a single layer of cells enclosing a large lumen. Epithelial cells of the principal salivary gland vary from cubic to columnar shape, with one or two spherical and well-developed nuclei. Cells of the anterior lobe of the principal salivary gland have an apical surface with narrow, short, and irregular plasma membrane foldings; apical and perinuclear cytoplasm rich in rough endoplasmic reticulum; and mitochondria with tubular cristae. The basal portion of the secretory cells has mitochondria associated with many basal plasma membrane infoldings that are short but form large extracellular canals. Secretory granules with electron-dense core and electron-transparent peripheral are dispersed throughout the cytoplasm. Cells of the posterior lobe of the principal salivary gland are similar to those of the anterior lobe, except for the presence of mitochondria with transverse cristae. The accessory salivary gland cells are columnar with apical microvilli, have well-developed nucleus and cytoplasm rich in rough endoplasmic reticulum, and have secretory granules. Cytochemical tests showed positive reactions for carbohydrate, protein, and acid phosphatase in different regions of the glandular system. The principal salivary glands of P. nigrispinus do not have muscle cells attached to its wall, suggesting that saliva-releasing mechanism may occurs with the participation of some thorax muscles. The cytochemical and ultrastructural features suggest that the principal and accessory salivary glands play a role in protein synthesis of the saliva.     

Ultrastructural alterations in branchial chloride cells of Atlantic salmon, Salmo salar, during parr-smolt transformation and early development in sea water

The ultrastructure of the gill primary lamellae of juvenile Atlantic salmon was examined during the parr-smolt transformation and for 42 days after smolts were exposed to sea water. Scanning electron microscopy indicated that primary lamellae were characterized by rough convoluted surfaces that became rougher throughout the experimental period and that crypts did begin to form in freshwater fish. Crypt formation increased in sea water.
Transmission electron microscopy indicated that parr preadapt for life in sea water in part by changes in chloride cells. Chloride cells show an elaboration of rough endoplasmic reticulum in fresh water and a decline of rough endoplasmic reticulum after 42 days of sea water exposure. The tubular membrane system becomes well developed in fresh water, and apical vesicles become abundant only after seawater exposure. Mitochondria are both spherical and elongate through the period and contain well developed cristae. No evidence of mitochondrial rupture was observed. The junctions between chloride cells and adjacent cells were characterized in fresh water by long tight junctions with desmosomes. This type of junction continued in sea water and was the norm between chloride cells and accessory cells after 42 days of seawater exposure. While leaky junctions appeared to be forming, no evidence was found of membrane interdigitation between accessory cells and chloride cells after 42 days of seawater exposure. It also appeared that seawater exposure influenced the number of chloride cells exposed to the external milieu.
Pavement cells showed an elaboration in fresh water of free ribosomes and rough endoplasmic reticulum and these elements became less prominent after seawater exposure.     

Characterization of the ultrastructure of gingival mast cells in alloxan-induced diabetic rats

The morphological changes of gingival mast cells of alloxan-induced diabetic rats were studied by electron microscopy. The following observations were made. The cell nucleus and cytoplasm degenerated. The electron density of the granules in the cell cytoplasm clearly decreased. Some granules had dense irregular threads and the granules were surrounded by a thin vacuole. A ghost vacuole formed in some mast cells and disorganized materials accumulated in the cytoplasm. The mast cell nuclei were generally irregular and degenerating mast cells had pyknotic nuclei. General destruction of the cell membrane and granule shedding in some samples was noted and mitochondria with atypical cristae in the cytoplasm of the mast cells were seen. We conclude that the characteristics of the ultrastructure of gingival mast cells in diabetics are distinctive and should be used as criteria for pathogenesis of gingival inflammation.     

Effects of glucose starvation on mitochondrial subpopulations in the meristematic and submeristematic regions of maize root

Mitochondria isolated from 3-mm long maize (Zea mays L. var Dea) root tips were found to be heterogeneous on Percoll density gradients. The ultrastructure of these isolated mitochondria correlated well with that of mitochondria observed in situ and was consistent with the existence of mitochondria at different stages of maturation during cell development. The mitochondria of higher density presented an ultrastructure with many cristae and a dense matrix. These mitochondria showed classic respiratory properties, although with low ADP/O ratios. In contrast, the mitochondria of lower density showed few cristae and a clear matrix and did not seem to be fully functional because their rate of respiration was low and showed weak respiratory control. Lower- and higher- density mitochondria were shown to be differentially affected during the first stages of glucose starvation. The higher-density mitochondria from glucose-starved maize root tips retained the ultrastructure and most of the respiratory properties of nonstarved mitochondria, whereas lower- and intermediate-density mitochondria were absent in the mitochondrial preparations from glucose-starved maize root tips and were not observed in situ. Quantitatively, there was a decrease of the total mitochondrial pool when expressed as the amount of mitochondrial protein per root tip. However, this decrease affected low- and intermediate-density mitochondria, but not higher-density mitochondria. Thus, it was shown that a significant pool of functional mitochondria is maintained in maize root tips during the first stages of glucose starvation. The reasons for these apparently selective effects of glucose starvation on mitochondria are discussed in relation to effects on mitotic and differentiation processes.