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1.
Gen Comp Endocrinol ; 143(2): 121-8, 2005 Sep 01.
Article in English | MEDLINE | ID: mdl-16061070

ABSTRACT

Day length predicts changing of seasons at mid-latitudes, but additional environmental cues (e.g., temperature, rainfall) give more precise information about timing of food peaks critical for offspring survival. We tested the effects of temperature on seasonal reproductive development of male song sparrows (Melospiza melodia morphna) from two populations: the Western Washington coast (3 m) and Cascade Mountains (500-1220 m). Previous work has shown that the timing of gonadal recrudescence can differ between the two sites in the field by as much as two months. However, in the laboratory under identical controlled conditions, testes grow at the same rate. To test whether temperature alone could account for a portion of the variation we measured in the field, we captured birds from each site and held them in temperature controlled environmental chambers that mimicked temperatures experienced either in the mountains or on the coast. We increased day length on a natural schedule, and measured testis volume, levels of circulating androgens and prolactin, and song rates. Increasing day length stimulated gonadal growth in all groups. We found only modest effects of temperature on reproductive development. In the mountain birds colder, montane temperatures slowed rates of growth, delaying the onset of growth by one month. Since temperature changes more markedly during the early winter months in the mountains than on the coast, increasing temperature may be a more relevant cue in timing of reproduction in the mountain population. These data suggest that while temperature helps to explain some of the variation in reproductive timing of free living sparrows, another as yet untested cue in the field may play a more important role. Furthermore, our data suggest that individuals within the same species may rely on different proximate cues for reproductive timing depending on the specific habitat in which they live.


Subject(s)
Reproduction/physiology , Seasons , Songbirds/growth & development , Temperature , Testis/growth & development , Analysis of Variance , Androgens/blood , Animals , Cues , Environment , Female , Male , Organ Size , Ovary/anatomy & histology , Photoperiod , Prolactin/blood , Songbirds/anatomy & histology , Statistics, Nonparametric , Testis/anatomy & histology , Vocalization, Animal/physiology
2.
J Neurosci ; 25(1): 10-8, 2005 Jan 05.
Article in English | MEDLINE | ID: mdl-15634762

ABSTRACT

Ependymal cells on the walls of brain ventricles play essential roles in the transport of CSF and in brain homeostasis. It has been suggested that ependymal cells also function as stem cells. However, the proliferative capacity of mature ependymal cells remains controversial, and the developmental origin of these cells is not known. Using confocal or electron microscopy (EM) of adult mice that received bromodeoxyuridine (BrdU) or [3H]thymidine for several weeks, we found no evidence that ependymal cells proliferate. In contrast, ependymal cells were labeled by BrdU administration during embryonic development. The majority of them are born between embryonic day 14 (E14) and E16. Interestingly, we found that the maturation of ependymal cells and the formation of cilia occur significantly later, during the first postnatal week. We analyzed the early postnatal ventricular zone at the EM and found a subpopulation of radial glia in various stages of transformation into ependymal cells. These cells often had deuterosomes. To directly test whether radial glia give rise to ependymal cells, we used a Cre-lox recombination strategy to genetically tag radial glia in the neonatal brain and follow their progeny. We found that some radial glia in the lateral ventricular wall transform to give rise to mature ependymal cells. This work identifies the time of birth and early stages in the maturation of ependymal cells and demonstrates that these cells are derived from radial glia. Our results indicate that ependymal cells are born in the embryonic and early postnatal brain and that they do not divide after differentiation. The postmitotic nature of ependymal cells strongly suggests that these cells do not function as neural stem cells in the adult.


Subject(s)
Ependyma/cytology , Ependyma/embryology , Neuroglia/physiology , Stem Cells/physiology , Age Factors , Amino Acid Transport System X-AG/analysis , Animals , Bromodeoxyuridine , Cell Differentiation , Cell Lineage , Cell Nucleus/ultrastructure , Cilia/ultrastructure , Ependyma/ultrastructure , Glutamate Plasma Membrane Transport Proteins , Immunohistochemistry , Male , Mice , Mitosis , Neuroglia/ultrastructure , Organelles/ultrastructure , S100 Proteins/analysis , Symporters/analysis , Thymidine/metabolism , Time Factors , Tritium
3.
Proc Natl Acad Sci U S A ; 101(50): 17528-32, 2004 Dec 14.
Article in English | MEDLINE | ID: mdl-15574494

ABSTRACT

Neural stem cells with the characteristics of astrocytes persist in the subventricular zone (SVZ) of the juvenile and adult brain. These cells generate large numbers of new neurons that migrate through the rostral migratory stream to the olfactory bulb. The developmental origin of adult neural stem cells is not known. Here, we describe a lox-Cre-based technique to specifically and permanently label a restricted population of striatal radial glia in newborn mice. Within the first few days after labeling, these radial glial cells gave rise to neurons, oligodendrocytes, and astrocytes, including astrocytes in the SVZ. Remarkably, the rostral migratory stream contained labeled migratory neuroblasts at all ages examined, including 150-day-old mice. Labeling dividing cells with the S-phase marker BrdUrd showed that new neurons continue to be produced in the adult by precursors ultimately derived from radial glia. Furthermore, both radial glia in neonates and radial glia-derived cells in the adult lateral ventricular wall generated self-renewing, multipotent neurospheres. These results demonstrate that radial glial cells not only serve as progenitors for many neurons and glial cells soon after birth but also give rise to adult SVZ stem cells that continue to produce neurons throughout adult life. This study identifies and provides a method to genetically modify the lineage that links neonatal and adult neural stem cells.


Subject(s)
Aging/physiology , Cell Differentiation , Neuroglia/cytology , Neurons/cytology , Stem Cells/cytology , Animals , Animals, Newborn , Brain/cytology , Cell Lineage , Mice , Microscopy, Electron
4.
Biol Reprod ; 71(3): 987-92, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15163618

ABSTRACT

Caloric restriction and hormone treatment delay reproductive senescence in female mammals, but a natural model of decelerated reproductive aging does not presently exist. In addition to describing such a model, this study shows that an abiotic signal (photoperiod) can induce physiological changes that slow senescence. Relative to animals born in April, rodents born in September delay their first reproductive effort by up to 7 mo, at which age reduced fertility is expected. We tested the hypothesis that the shorter day lengths experienced by late-born Siberian hamsters ameliorate the reproductive decline associated with advancing age. Short-day females (10L:14D) achieved puberty at a much later age than long-day animals (14L:10D) and had twice as many ovarian primordial follicles. At 10 mo of age, 86% of females previously maintained in short day lengths produced litters, compared with 58% of their long day counterparts. Changes in pineal gland production of melatonin appear to mediate the effects of day length on reproductive aging; only 30% of pinealectomized females housed in short days produced litters. Exposure to short days induces substantial decreases in voluntary food intake and body mass, reduced ovarian estradiol secretion, and enhanced production of melatonin. One or more of these changes may account for the protective effect of short day lengths on female reproduction. In delaying reproductive senescence, the decrease in day length after the summer solstice is of presumed adaptive significance for offspring born late in the breeding season that first breed at an advanced chronological age.


Subject(s)
Aging/physiology , Photoperiod , Reproduction/physiology , Animals , Cricetinae , Female , Male , Melatonin/physiology , Phodopus , Pineal Gland/physiology , Pineal Gland/surgery , Pregnancy , Seasons
5.
Oecologia ; 140(2): 201-10, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15148599

ABSTRACT

Seasonal temperate zone breeders respond to increasing day length to anticipate the approach of spring breeding conditions. Other (supplementary) environmental cues, such as temperature and precipitation, were historically thought to play unimportant roles in reproductive timing. We demonstrate variation in reproductive timing across small geographic distances by examining the vernal testicular recrudescence of adult song sparrows (Melospiza melodia morphna) breeding in coastal (0-10 m elevation) and montane (280-1220 m elevation) habitats. Each year, these birds experienced the same photoperiod, but were exposed to different supplementary cues that varied with altitude. Coastal birds experienced warmer and more stable temperatures during late winter and early spring than did montane birds. We measured bud opening, emergence of new green shoots, and arthropod biomass to monitor the pace of spring's approach. New spring shoots emerged 2 months earlier on the coast than in the mountains and buds on flowering trees and shrubs also tended to open earlier at the coast. Arthropod biomass was similar in both the mountains and the coast during early spring, and began to increase in early summer. Reproductive morphology (i.e. testis volume and cloacal protuberance length) developed up to 2 months earlier on the coast than in the mountains. Testicular recrudescence occurred earlier on the coast in most years and proceeded at a faster rate in 1 year. Circulating levels of luteinizing hormone, follicle stimulating hormone and prolactin increased through the season, but did not correlate with differences between sites. Both populations responded similarly when exposed to identical photoperiodic cues in the laboratory. Therefore, we suggest that an integrated response to cues characteristic of location and elevation account for differences in patterns measured in the field.


Subject(s)
Altitude , Reproduction/physiology , Seasons , Sparrows/growth & development , Testis/physiology , Analysis of Variance , Animals , Follicle Stimulating Hormone/blood , Geography , Luteinizing Hormone/blood , Male , Organ Size , Prolactin/blood , Temperature , Time Factors , Washington
6.
Nature ; 427(6976): 740-4, 2004 Feb 19.
Article in English | MEDLINE | ID: mdl-14973487

ABSTRACT

The subventricular zone (SVZ) is a principal source of adult neural stem cells in the rodent brain, generating thousands of olfactory bulb neurons every day. If the adult human brain contains a comparable germinal region, this could have considerable implications for future neuroregenerative therapy. Stem cells have been isolated from the human brain, but the identity, organization and function of adult neural stem cells in the human SVZ are unknown. Here we describe a ribbon of SVZ astrocytes lining the lateral ventricles of the adult human brain that proliferate in vivo and behave as multipotent progenitor cells in vitro. This astrocytic ribbon has not been observed in other vertebrates studied. Unexpectedly, we find no evidence of chains of migrating neuroblasts in the SVZ or in the pathway to the olfactory bulb. Our work identifies SVZ astrocytes as neural stem cells in a niche of unique organization in the adult human brain.


Subject(s)
Astrocytes/cytology , Brain/cytology , Cell Movement , Multipotent Stem Cells/cytology , Neurons/cytology , Adult , Astrocytes/ultrastructure , Autopsy , Biopsy , Brain/ultrastructure , Cell Differentiation , Cell Division , Cells, Cultured , Humans , Multipotent Stem Cells/ultrastructure , Neurons/ultrastructure , Olfactory Bulb/cytology , Olfactory Bulb/ultrastructure
7.
J Neurobiol ; 58(3): 413-22, 2004 Feb 15.
Article in English | MEDLINE | ID: mdl-14750153

ABSTRACT

Songbirds show dramatic neural plasticity as adults, including large-scale anatomical changes in discrete brain regions ("song control nuclei") controlling the production of singing behavior. The volumes of several song control nuclei are much larger in the breeding season than in the nonbreeding season, and these seasonal neural changes are regulated by plasma testosterone (T) levels. In many cases, the effects of T on the central nervous system are mediated by neural conversion to estradiol (E(2)) by the enzyme aromatase. The forebrain of male songbirds expresses very high levels of aromatase, in some cases adjacent to song control nuclei. We examined the effects of aromatase inhibition and estrogen treatment on song nuclei size using wild male songbirds in both the breeding and nonbreeding seasons. In breeding males, aromatase inhibition caused the volume of a telencephalic song control nucleus (HVC) to decrease, and this effect was partially rescued by concurrent estrogen replacement. In nonbreeding males, estradiol treatment caused HVC to grow to maximal spring size within 2 weeks. Overall, these data suggest that aromatization of T is an important mediator of song control system plasticity, and that estradiol has neurotrophic effects in adult male songbirds. This study demonstrates that estrogen can affect adult neural plasticity on a gross anatomical scale and is the first examination of estrogen effects on the brain of a wild animal.


Subject(s)
Brain/growth & development , Estrogens/metabolism , Neuronal Plasticity/physiology , Sexual Behavior, Animal/physiology , Songbirds/metabolism , Vocalization, Animal/physiology , Animals , Aromatase/metabolism , Aromatase Inhibitors , Brain/cytology , Brain/enzymology , Enzyme Inhibitors/pharmacology , Estrogens/pharmacology , Male , Neural Pathways/cytology , Neural Pathways/enzymology , Neural Pathways/growth & development , Neuronal Plasticity/drug effects , Neurons/cytology , Neurons/drug effects , Neurons/enzymology , Seasons , Sexual Behavior, Animal/drug effects , Songbirds/anatomy & histology , Telencephalon/cytology , Telencephalon/enzymology , Telencephalon/growth & development , Testosterone/metabolism , Vocalization, Animal/drug effects
8.
J Neurobiol ; 57(2): 130-40, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14556279

ABSTRACT

In seasonally breeding songbirds, the brain regions that control song behavior undergo dramatic structural changes at the onset of each annual breeding season. As spring approaches and days get longer, gonadal testosterone (T) secretion increases and triggers the growth of several song control nuclei. T can be converted to androgenic and estrogenic metabolites by enzymes expressed in the brain. This opens the possibility that the effects of T may be mediated via the androgen receptor, the estrogen receptor, or both. To test this hypothesis, we examined the effects of two bioactive T metabolites on song nucleus growth and song behavior in adult male white-crowned sparrows. Castrated sparrows with regressed song control nuclei were implanted with silastic capsules containing either crystalline T, 5alpha-dihydrotestosterone (DHT), estradiol (E(2)), or a combination of DHT+E(2). Control animals received empty implants. Song production was highly variable within treatment groups. Only one of seven birds treated with E(2) alone was observed singing, whereas a majority of birds with T or DHT sang. After 37 days of exposure to sex steroids, we measured the volumes of the forebrain song nucleus HVc, the robust nucleus of the archistriatum (RA), and a basal ganglia homolog (area X). All three steroid treatments increased the volumes of these three song nuclei when compared to blank-implanted controls. These data demonstrate that androgen and estrogen receptor binding are sufficient to trigger seasonal song nucleus growth. These data also suggest that T's effects on seasonal song nucleus growth may depend, in part, upon enzymatic conversion of T to bioactive metabolites.


Subject(s)
Androgens/pharmacology , Brain/anatomy & histology , Estrogens/pharmacology , Songbirds/physiology , Vocalization, Animal/physiology , Androgens/blood , Animals , Brain/drug effects , Brain/physiology , Dihydrotestosterone/blood , Dihydrotestosterone/pharmacology , Estradiol/blood , Estradiol/pharmacology , Estrogens/blood , Male , Neuronal Plasticity/drug effects , Neuronal Plasticity/physiology , Orchiectomy , Seasons , Vocalization, Animal/drug effects
9.
Cereb Cortex ; 13(6): 580-7, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12764031

ABSTRACT

The germinal neuroepithelium, or ventricular zone (VZ) of the developing fetal brain, was once thought to transform into the non-germinal ependymal zone of the postnatal and adult brain. Persistence of neural stem cells and neurogenesis throughout postnatal life, however, suggests a continuum between embryonic and adult germinal brain centers. Here, we suggest that developmental changes in anatomy and molecular marker expression in the ventricular walls (the principal germinal centers of the brain) may have misled us into current interpretations of VZ transformation from a germinal to a non-germinal epithelium. We review previous studies and present new data indicating that a germinal layer with characteristics similar to those of the embryonic VZ persists in lateral ventricular walls of the postnatal mouse brain, a region where the adult subventricular zone (SVZ) develops and where neurogenesis persists into adult life. The early postnatal VZ is largely composed of radial glial cell bodies that remain proliferative, display interkinetic nuclear migration and serve as progenitors of new neurons. Ependymal cells then progressively populate the walls of the lateral ventricle but a subpopulation of astrocytes, derived from radial glia, remain in contact with the ventricle lumen, into which they extend a single cilium similar to that found on neuroepithelial cells and radial cells. We propose that a VZ 'compartment' is retained postnatally and that this niche may be essential for stem cell function.


Subject(s)
Cerebral Ventricles/cytology , Cerebral Ventricles/growth & development , Neuroglia/cytology , Neuroglia/physiology , Stem Cells/cytology , Animals , Animals, Newborn , Cell Differentiation/physiology , Cerebral Ventricles/embryology , Cerebral Ventricles/physiology , Mice , Neurons/cytology , Neurons/physiology , Stem Cells/physiology
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