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Featured researches published by Kazue Mogi.


Fluids and Barriers of the CNS | 2012

Visualisation of cerebrospinal fluid flow patterns in albino Xenopus larvae in vivo.

Kazue Mogi; Takeshi Adachi; Susumu Izumi; Ryuji Toyoizumi

BackgroundIt has long been known that cerebrospinal fluid (CSF), its composition and flow, play an important part in normal brain development, and ependymal cell ciliary beating as a possible driver of CSF flow has previously been studied in mammalian fetuses in vitro. Lower vertebrate animals are potential models for analysis of CSF flow during development because they are oviparous. Albino Xenopus laevis larvae are nearly transparent and have a straight, translucent brain that facilitates the observation of fluid flow within the ventricles. The aim of these experiments was to study CSF flow and circulation in vivo in the developing brain of living embryos, larvae and tadpoles of Xenopus laevis using a microinjection technique.MethodsThe development of Xenopus larval brain ventricles and the patterns of CSF flow were visualised after injection of quantum dot nanocrystals and polystyrene beads (3.1 or 5.8 μm in diameter) into the fourth cerebral ventricle at embryonic/larval stages 30-53.ResultsThe fluorescent nanocrystals showed the normal development of the cerebral ventricles from embryonic/larval stages 38 to 53. The polystyrene beads injected into stage 47-49 larvae revealed three CSF flow patterns, left-handed, right-handed and non-biased, in movement of the beads into the third ventricle from the cerebral aqueduct (aqueduct of Sylvius). In the lateral ventricles, anterior to the third ventricle, CSF flow moved anteriorly along the outer wall of the ventricle to the inner wall and then posteriorly, creating a semicircle. In the cerebral aqueduct, connecting the third and fourth cerebral ventricles, CSF flow moved rostrally in the dorsal region and caudally in the ventral region. Also in the fourth ventricle, clear dorso-ventral differences in fluid flow pattern were observed.ConclusionsThis is the first visualisation of the orchestrated CSF flow pattern in developing vertebrates using a live animal imaging approach. CSF flow in Xenopus albino larvae showed a largely consistent pattern, with the exception of individual differences in left-right asymmetrical flow in the third ventricle.


Laterality | 2009

Optic chiasm in the species of order Clupeiformes, family Clupeidae: Optic chiasm of Spratelloides gracilis shows an opposite laterality to that of Etrumeus teres

Kazue Mogi; Kazuya Misawa; Kentaro Utsunomiya; Yuta Kawada; Toshihisa Yamazaki; Shigeo Takeuchi; Ryuji Toyoizumi

In most teleost fishes, the optic nerves decussate completely as they project to the mesencephalic region. Examination of the decussation pattern of 25 species from 11 different orders in Pisces revealed that each species shows a specific chiasmic type. In 11 species out of the 25, laterality of the chiasmic pattern was not determined; in half of the individuals examined, the left optic nerve ran dorsally to the right optic nerve, while in the other half, the right optic nerve was dorsal. In eight other species the optic nerves from both eyes branched into several bundles at the chiasmic point, and intercalated to form a complicated decussation pattern. In the present study we report our findings that Spratelloides gracilis, of the order Clupeiformes, family Clupeidae, shows a particular laterality of decussation: the left optic nerve ran dorsally to the right (n=200/202). In contrast, Etrumeus teres, of the same order and family, had a strong preference of the opposite (complementary) chiasmic pattern to that of S. gracilis (n=59/59), revealing that these two species display opposite left–right optic chiasm patterning. As far as we investigated, other species of Clupeiformes have not shown left–right preference in the decussation pattern. We conclude that the opposite laterality of the optic chiasms of these two closely related species, S. gracilis and E. teres, enables investigation of species-specific laterality in fishes of symmetric shapes.


Cells Tissues Organs | 2010

Invasion by Matrix Metalloproteinase-Expressing Cells Is Important for Primitive Streak Formation in Early Chick Blastoderm

Kazue Mogi; Ryuji Toyoizumi

Epiblast cells in the early chick embryo differentiate to form all three germ layers through ingression of cells at the primitive streak across the basement membrane that underlies the epiblast. We tested the idea that degradation of the extracellular matrix components by matrix metalloproteinase(s) (MMPs) is involved in this process. Epiblast cells and primitive streak cells were dissociated into single cells and seeded onto a reconstituted basement membrane gel in vitro. Following overnight culture, approximately half the cells made holes in the substratum by dissolving the gel matrix. This invasive phenomenon was reproduced in vitro even when the cells were cultured upside down using a hanging culture system. We detected gelatinase activity in the culture supernatants from both prestreak epiblast cells and primitive streak cells. Pro-MMP-2 was detected in the culture media of the prestreak/streak cells as a 72-kDa band by gelatin zymography. In RT-PCR experiments, mRNAs for MMP-2, membrane-type (MT)3-MMP and MMP-11(stromelysin-3) were expressed in the epiblast cells before and during primitive streak formation. Injection of GM 6001 or other MMP inhibitors into the subgerminal cavity of the embryo inhibited the formation of the primitive streak and/or the primitive groove in more than 82% of the injected embryos. On the other hand, injection of a negative control compound instead of GM 6001 did not cause substantial inhibition. These results suggest that MMPs are involved in the enzymatic degradation of the basement membrane underlying the epiblast and are thus important for the ingression of mesendodermal cells along the primitive streak.


Archive | 2018

Left–Right Specification in the Embryonic and Larval Development of Amphibians

Ryuji Toyoizumi; Kazue Mogi

Biomolecules in living organisms, such as amino acids and double-stranded DNA, show left–right asymmetry. Even unicellular organisms, such as ciliates, have species-specific left- or right-handedness. Such molecular chiral asymmetry and cellular left–right asymmetry have likely provided a basis for the evolution of genetically determined left–right asymmetry of organ situs and the morphology of the heart, visceral organs, and central nervous system in eumetazoans. To study left–right asymmetry of the body plan, we believe that Xenopus laevis is a valuable model organism. The early Xenopus larva forms a transparent epidermis in the ventral abdominal region; thus organ development and morphology can be easily observed without dissection.


The International Journal of Developmental Biology | 2005

Xenopus nodal related-1 is indispensable only for left-right axis determination

Ryuji Toyoizumi; Tsuyoshi Ogasawara; Shigeo Takeuchi; Kazue Mogi


Developmental Biology | 2000

More than 95% reversal of left-right axis induced by right-sided hypodermic microinjection of activin into Xenopus neurula embryos.

Ryuji Toyoizumi; Kazue Mogi; Shigeo Takeuchi


The International Journal of Developmental Biology | 2003

Xenopus neurula left-right asymmetry is respeficied by microinjecting TGF-beta5 protein.

Kazue Mogi; Madoka Goto; Eri Ohno; Yoshitaka Azumi; Shigeo Takeuchi; Ryuji Toyoizumi


The International Journal of Developmental Biology | 2000

Correlation between the expression of the HNK-1 epitope and cellular invasiveness in prestreak epiblast cells of chick embryos.

Kazue Mogi; Ryuji Toyoizumi; Shigeo Takeuchi


The Japanese Biochemical Society/The Molecular Biology Society of Japan | 2015

Xenopus fin-shape morphogenesis is controlled by antagonistic BMP signaling and Wnt signaling

Kotomi Imura; Kazue Mogi; Yuki Sugiura; Shinya Tsuruoka; Tsuyoshi Kobayashi; Hideho Uchiyama; Ryuji Toyoizumi


Science Journal of Kanagawa University | 2013

2012年度神奈川大学総合理学研究所共同研究助成論文 アフリカツメガエル Xenopus laevisと洞窟魚 Astyanax mexicanusの初期発生に対するSonic hedgehog経路阻害剤SANT-1投与の影響

真実 前田; Manami Maeda; 和枝 茂木; Kazue Mogi; 剛 小林; Tsuyoshi Kobayashi; 晶也 日野; Akiya Hino; 龍児 豊泉; Ryuji Toyoizumi

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