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Biomedical subjects

A LaVelle

Publications and source records attributed to A LaVelle.

At least 19 recordsLinked to original sources
PubMed1993

Metabolic changes in axotomized fetal and early postnatal hamster facial motoneurons: an autoradiographic study.

The developing facial neurons of a series of hamsters ranging in age from the 14-day fetus to the 9 day postnatal were axotomized. Postoperative times were graded for each age so that the retrograde response could be observed before any significant amount of cell degeneration or death occurred. The incorporation of tritiated uridine was followed by the autoradiographic procedure. Although grain counts, relative to control values, were significantly reduced only in the axotomized fetus and at 24 hours postoperatively in 4-day postnatal animals, there was also a repression of isotopic incorporation in all the other axotomized animals. These results support data obtained from previous work with the hamsters which indicate that it is not until after the nerve cell nucleolus reaches full cytomorphic maturity (between 15 and 20 days postnatal age in hamster facial neurons) that the axotomized neurons respond with significantly increased incorporation levels of isotope over that of control neurons.

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PubMed1992

Alterations in nuclear envelope invaginations in axotomized fetal and early postnatal hamster facial motoneurons.

In this study, changes in the amount of nuclear envelope invaginations (NEI) were morphometrically assessed after axotomy during late fetal and early postnatal developmental stages in hamster facial motoneurons. These changes were expressed as boundary density or BA (length of nuclear envelope per unit area of nucleus). Axotomy-induced changes in nuclear area and perimeter were also quantitatively determined. At 17 h after axotomy in the fetal operative series, no changes in any of the parameters were seen. At 1 day postoperative (dpo) in newborn, 2 and 4 postnatal day animals, the boundary densities of the total and invaginated portion of the nuclear envelope increased significantly. No corresponding qualitative changes were observed. At 2 dpo in 4 and 7 postnatal day animals, there were significant increases in the boundary densities of both invaginated and total nuclear envelope and a decrease in nuclear area. These changes were not seen at 2 dpo in the 9-day operative series. At 4 dpo in 7 and 9 postnatal day animals, scalloping of the normally smooth nuclear profile, as well as a flattening and elongation in nuclear shape, occurred. These qualitative changes in the 7 and 9 day operated groups were also accompanied by significant changes in all the measured parameters. The boundary density of the invaginated, non-invaginated and total nuclear envelope increased; whereas, nuclear area and perimeter decreased. These results argue against the generally held hypothesis that an increase in nuclear envelope invaginations is indicative of an allied increase in cellular metabolism.(ABSTRACT TRUNCATED AT 250 WORDS)

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PubMed1991

Ultrastructural changes in the nucleolus of facial motor neurons following axotomy during an early critical period in development.

In this study, the effects of axotomy on the ultrastructure of the nucleolus and associated organelles were examined in fetal, newborn, and early postnatal facial motoneurons of the hamster. Golden hamsters used for this study were the 14-day fetus, newborn (0 days; less than 6 hr) and 2, 4, 7, and 9 days postnatal ages, with 3 animals per group. For prenatal surgeries, pregnant hamsters were anesthetized and the facial nerves severed in the fetuses via electrocautery through the uterine wall and amniotic membrane. For postnatal surgeries, the animals were anesthetized and the right facial nerve exposed and severed at its exit from the stylomastoid foramen. At the appropriate postoperative times, the animals were reanesthetized and perfused-fixed. The facial nuclear groups were dissected and processed for routine electron microscopy. Microbody and coiled body frequencies were determined from the number of neurons containing these structures per number of neurons sampled per animal in each experimental or control group and subjected to statistical analysis. Nucleolar reactive changes that occurred during this developmental sequence fell into two major categories. The first category displayed by most injured cells consisted of an initial compacting of fibrillar material and reduction in vacuolar space. The second category appeared to represent a progression from this first stage of nucleolar reactivity into degenerative changes involving a striking segregation of nucleolar components into five distinct regions. The incidence of microbodies increased as a result of axotomy, whereas the presence of coiled bodies decreased at the later postoperative stages in the older animals. With increasing age and nucleolar maturation, the nucleolar reactive pattern became less pronounced and severe, and neuronal survival predominated. It appears, therefore, that the two categories of nucleolar changes following axotomy during early development correlate with changes observed in nucleoli under conditions of rRNA downregulation. It is hypothesized from these results that a key step in the ability of neurons to survive axotomy and successfully regenerate at these early developmental stages occurs at some point in ribosomal RNA transcription and/or processing. Complementary information at the molecular level concerning changes in nucleolar synthetic activity and ribosome production will be necessary to test this hypothesis.

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PubMed1990

Ultrastructural and morphometric analysis of nucleolar and nuclear changes during the early growth period in hamster facial neurons.

In this study, progressive developmental changes in the nucleus and associated organelles, including the nucleolus, coiled bodies, nuclear envelope, and nucleoplasm, of hamster facial motor neurons were characterized by two parallel analyses: ultrastructural and morphometric. Golden hamsters (Mesocricetus auratus) used for this series were the 14-day fetus, newborn (less than 6 hr), and 1, 2, 3, 4, 5, 7, 9, 11 and 13 days postnatal ages, with 3 animals per group. Following anesthesia and perfusion fixation, facial nuclear groups were dissected and processed for electron microscopy. Electron micrographs and camera lucida tracings of nuclear profiles were collected and analyzed. The ultrastructural analysis revealed progressive changes in the nucleolus from a compact, segregated type to a reticulated form characteristic of actively protein-secreting cells. Nucleolar microbodies and fibrillar centers were seen at all ages; the latter structures appeared to decrease in size and increase with age in the series. The nucleolus-associated chromatin became less condensed, suggesting an increase in the incorporation of rDNA into the nucleolus proper. Coiled bodies, both free and attached to nucleoli, were found in varying frequencies. The nucleoplasm of neurons at the earliest stages contained large numbers of heterochromatin clumps, which decreased concomitantly with an increase in interchromatin granules and fibrils during the later stages. Nuclear envelope invaginations, polarized along one side of the nucleus, increased throughout the developmental period examined. These changes occurred in concert with a 61% increase in nuclear size and a 47% increase in the length of nuclear envelope. The sequence of nuclear changes observed during this early period of normal facial neuronal growth completes the study of a series of distinctly defined cytomorphic events in this cell type, the lability of which can be experimentally tested for their functional roles in neuronal development.

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PubMed1987

Differential effects of axotomy on immature and mature hamster facial neurons: a tritiated-uridine autoradiographic study.

In this study, tritiated-uridine incorporation was autoradiographically examined following axotomy of hamster facial motor neurons (HFMN) at the critical development age of 15 days postnatal and in the adult. The postoperative times selected were 0.5, 1, 2, and 4 days. In the 15-day operative series, no changes in incorporation were observed at any of the postoperative times, except at 4 days postoperative, when there was a decrease in tritiated-uridine incorporation in the axotomized neurons relative to the controls. In the adult operative series there were no changes in incorporation at 0.5 or 1 day postoperative, relative to the controls. At 2 days postoperative in the adult, there was a transient increase in tritiated-uridine incorporation that returned to control levels by 4 days postoperative. When axotomized and control cytoplasmic/nuclear grain densities were compared, no changes were found in either operative series. These results of the time course of axotomy-induced changes in RNA synthesis in HFMN corroborate our previous findings of an age-dependent reactive sequence in HFMN and lend support to the hypothesis that the young neurons are synthesizing at peak capacity related to final growth and cannot be stimulated further by axotomy. As discussed, the transient increase in RNA levels in the adult, the lack of any changes in the rate of transfer of RNA from the nucleus to the cytoplasm, and the decrease in RNA levels in the 15-day neurons may be related to the presence of an unusual intranucleolar body within the nucleolus of HFMN that contains ribosomal precursors.

Aging↗
PubMed1986

Ultrastructural changes in the nucleoplasm of hamster facial neurons during a postnatal maturation period.

Changes in the characteristics of the nucleoplasm were examined in young hamster facial motoneurons of 15 and 20 days postnatal age and in the adult (100 days postnatal age) at both the light and electron microscope levels. In toluidine-blue stained 1-micron thick sections, a progressive increase in basophilic islands within the nucleoplasm occurred during maturation. Ultrastructural changes that were observed during final development included a transition from a homogeneous, 'filled-in' appearing nucleoplasm to a clumped-appearing nucleoplasm. This process principally involved the formation of distinct clusters of interchromatin granules that was associated with a loss of fine fibrils, an increase in clear spaces between intervening fibrillar and granular material, and an increase in small scattered clumps of heterochromatin. These changes in both ribonucleoprotein (RNP)-and DNA-containing nuclear constituents (interchromatin granules and heterochromatin, respectively) occurred during a postnatal maturational period previously demonstrated to involve other alterations in nuclear structures. It is interpreted that these cytomorphic changes in the nucleoplasm reflect an underlying metabolic shift at the transcriptional level during the transition from an actively growing neuron to an adult functioning neuron.

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PubMed1985

An unusual nucleolar ring-like structure in axotomized hamster facial motoneurons.

Structures consisting of connecting rings surrounding a fibrillar core were observed within nucleoli of developing normal and axotomized hamster facial motoneurons. A few appeared in the nucleoplasm, attached to coiled bodies. Their peculiar structure and temporal association with neuronal maturation may reflect a transient state of ribosomal RNA transcription.

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PubMed1985

Changes in nuclear envelope invaginations in axotomized immature and mature hamster facial motoneurons.

In this study, changes in the amount of nuclear envelope invaginations (NEI) were quantitatively assessed after axotomy during the late nuclear maturation stages (15, 20 and 25 days postnatal age) and in the adult (100-day-old) hamster facial motoneurons. These changes were expressed as boundary density or BA (length of nuclear envelope per unit area of nucleus). Absolute nuclear areas and perimeters were also estimated after axotomy at these ages. At 1/2 and 1 day after axotomy, no differences in the above parameters were noted at any of the operative ages. At 4 days postoperative, the peak of chromatolysis for all these ages, axotomy resulted in significant decreases in BA and nuclear perimeter in the immature neurons and no changes in BA and nuclear perimeter in the adult neurons. In addition, 4 days after axotomy at 20 days postnatal and later ages, pronounced increases in nuclear area occurred. These quantitative results are interpreted as evidence that the accelerated loss of NEI after axotomy during the final stages of nuclear maturation in these neurons is related to the formation of rough endoplasmic reticulum (RER) or Nissl substance. The hypothesis that an 'excess' of RER is accumulated during the late maturation stages and may account for the lack of NEI in the adult axotomized facial motoneuron is presented.

Aging↗
PubMed1985

Some introductory comments on silver staining.

Silver staining has become a versatile method for the visualization of specific cell structures and products. The similarity of the impregnation "nuclei" of reduced silver staining to the silver "specks" or "nuclei" of the latent image in photography is noted. "Physical" development (reduction of ionic silver in solution) in silver staining as compared to "chemical" development (reduction of ionic silver remaining in a silver halide crystal) in photographic procedures is briefly discussed.

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PubMed1983

A difference in the nucleoli of Purkinje cells of the nodular lobe of the hamster cerebellum.

Purkinje cells of the hamster cerebellum typically contain a large, single, centrally located nucleolus. Strikingly different are Purkinje cells concentrated in the nodular cortex, which characteristically contain several small, pale-staining nucleoli, most of which are peripherally located, in contact with the nuclear envelope. These atypical cells are also smaller, their Nissl bodies stain less intensely, and their nuclear envelopes appear more invaginated. Functional differences are implicit.

Animals↗
PubMed1983

Nuclear envelope invaginations in hamster facial motor neurons during development and aging.

Morphometric measurements of nuclear envelope invaginations (NEI) in hamster facial motor neurons were made. These showed that the amount of NEI increased markedly between fetal life and birth to a high level that was maintained during the period of accelerated neuronal somal growth. Subsequently, the amount of NEI decreased to a plateau of low incidence that persisted through maturity and aging. This sequence of NEI formation and subsidence differs from that previously observed in a similar developing and aging series of pyramidal neurons in the same species. This may indicate, as discussed, that the presence of NEI reflects stage-specific functions that may differ depending on neuronal type.

Aging↗
PubMed1983

Morphometry of nuclei, nuclear envelopes and nucleoli in aging hamster cerebrum.

The neuronal nucleus and nucleolus undergo extensive dimensional and configurational changes during maturation and aging, as shown in this study of pyramidal cells of the hamster motor cortex. With maturation, the increase in nuclear perimeter length per unit nuclear area was associated with an increased amount of nuclear invaginations. With maturation and aging, there was a change in nuclear caliper shape, from spherical to very nonspherical. The number of nucleoli containing microbodies peaked first at 15 days and again at 600 days. It is concluded that area, perimeter and form factor relate to nuclear caliper shape and the presence of nucleolar microbodies. The correlated changes in these parameters appear to differentially reflect stage-specific metabolic conditions related to two critical phases: (1) an early phase (10-15 days) at the inception of configurational changes leading to maturity, and (2) a late phase (600-700 days) at the inception of configurational changes leading to old age.

Aging↗
PubMed1981

Morphological changes of the pyramidal cell nucleolus and nucleus in hamster frontal cortex during development and aging.

The development and aging of the nucleolus and nucleus in layer V pyramidal cells in the hamster cerebrum were studied by light and electron microscopy. The nucleoli appeared in the newborn as occasional fibrillar masses adjacent to peripherally placed bodies of chromatin. By maturity, a single, generally central, nucleolus proper with nucleolus-associated chromatin was present. Nucleolar microbodies were observed at 10, 15, 20 and 480 days, but not in the newborn, 5-or 90-day animal. An intranucleolar body was not observed at the electron at the electron-microscopy level in these pyramidal cell nucleoli at any age in this series, in contrast to the situation in large motor neurons of the facial nucleus. The nucleus progressed from an irregular shape at birth to an oval shape at maturity. At 10 days, incipient invaginations of the nuclear membrane appeared; these subsequently increased in depth and frequency in the adult. The above changes, particularly in the nucleoli, are correlated in time with changes involving the endoplasmic reticulum. The correlations may indicate different periods of metabolic activity in the hamster pyramidal neurons. Four such periods can be differentiated on the basis of cytomorphic changes which may be correlated to reported development of function. The sequence of these changes, peculiar to the developing and aging hamster pyramidal neuron, differs from that seen in large spinal and cranial motor neurons. It appears that some features of nuclear immaturity, which are lost in larger neuronal types, are retained in the adult pyramidal neuron.

Aging↗
PubMed1981

Tritiated leucine incorporation in the developing hamster facial nucleus with injury: a liquid scintillation study.

Tritiated leucine incorporation was examined after either crush or axotomy of the hamster facial nerve at specific stages in the maturation of the neuronal nucleolus. Changes in the neuronal metabolic response to injury in development were demonstrated with liquid scintillation examination of tritiated leucine incorporation into the trichloroacetic acid (TCA)-insoluble and TCA-soluble fractions derived from whole reactive and normal facial nuclear groups. Changes in incorporation seen in the developmental sequence were attributed to actual changes in neuronal protein metabolism, and not to changes in the amino acid pool, glial changes or hyperemic capillary changes. The ability to increase leucine incorporation over the normal as a result of injury in development coincided with the time of final nucleolar maturation in the facial motor neurons, beginning at approximately 20 days postnatal age. Thus, there is a correlation between a specific morphological event, the attainment of the mature nucleolar configuration, and the acquisition of the mature synthetic capacity as indicated by the ability to respond to injury in the mature manner.

Aging↗
PubMed1981

Nuclear envelope invaginations in hamster pyramidal cells during development and aging.

Nuclear envelope invaginations were observed in pyramidal cell nuclei of the hamster frontal cortex during development and aging. These invaginations which began to appear at 10 day did not recede at maturity as has been observed in certain other cell types, but persisted in the adult hamster and during subsequent aging. Morphometric data showed a significant increase in the number of nuclear envelope invaginations and in their length per unit of the nucleus. This increase was positively correlated with age until 500 days and is suggestive of a continued high metabolic activity that did not subside following the rapid growth phase of the pyramidal neurons.

Aging↗