Shuichi Obata

Shuichi Obata

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2007 in European Journal of Cell Biology
Verified
Journal Article
Closed access
Keiichiro YoshidaKeiichiro Yoshida
Keiichiro Yoshida
SOShuichi Obata
Shuichi Obata
MOMichio Ono
Michio Ono
MEMichiyo Esaki
Michiyo Esaki
TMTatsuo Maejima
Tatsuo Maejima
HSHajime Sawada
Hajime Sawada

1 January 2007 in The International Journal of Developmental Biology
Verified
Journal Article
Open access
KTKazuhiro Takano
Kazuhiro Takano
YIYuzuru Ito
Yuzuru Ito
SOShuichi Obata
Shuichi Obata
TOTsutomu Oinuma
Tsutomu Oinuma
SKShinji Komazaki
Shinji Komazaki
MAMakoto Asashima
Makoto Asashima
During vertebrate cardiac development, the heart tube formed by fusion of right and left presumptive cardiac mesoderms (PCMs) undergoes looping toward the right, resulting in an asymmetrical heart. Here, we examined the right and left PCMs with regard to heart-tube looping using right- and left-half newt embryos (Cynops pyrrhogaster ). In the half embryos, the rightward (normal) loop of the heart tube was formed from the left PCM, irrespective of the timing of its separation, while the leftward (reversed) loop of the heart tube was formed from the right PCM, separated by stage 18. In addition, the direction of the leftward loop was inverted to the rightward direction in right-half embryos bisected after stage 18. Incision or resection of the embryonic caudal region implicated interactions between the right and left sides of this region as crucial for inverting the direction of the heart-tube loop from leftward to rightward in the right-half embryos. In situ hybridization of CyNodal (Cynops nodal-related gene) suggested that the inversion of heart looping in the right-half embryos has no association with the CyNodal expression pattern. Based on these findings, we propose a mechanism for the rightward looping underlying normal amphibian cardiac development.

1 November 2022 in Biomedicines
Verified
Journal Article
Open access
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XCXutong Chen
Xutong Chen
RARyo Ando
Ryo Ando
RCRoman Martin Casco-Robles
Roman Martin Casco-Robles
MCMartin Miguel Casco-Robles
Martin Miguel Casco-Robles
FMFumiaki Maruo
Fumiaki Maruo
CCChikafumi Chiba
Chikafumi Chiba
In adult newts, when a limb is amputated, a mesenchymal cell mass called the blastema is formed on the stump, where blood vessels filled with premature erythrocytes, named polychromatic normoblasts (PcNobs), elongate. We previously demonstrated that PcNobs in the blastema express an orphan gene, Newtic1, and that they secrete growth factors such as BMP2 and TGFβ1 into the surrounding tissues. However, the relationship between Newtic1 expression and growth factor secretion was not clear since Newtic1 was thought to encode a membrane protein. In this study, we addressed this issue using morphological techniques and found that the Newtic1 protein is a component of globular structures that accumulate at the marginal band in the cytoplasm along the equator of PcNobs. Newtic1-positive (Newtic1(+)) globular structures along the equator were found only in PcNobs with a well-developed marginal band in the blastema. Newtic1(+) globular structures were associated with microtubules and potentially incorporated TGFβ1. Based on these observations, we propose a hypothesis that the Newtic1 protein localizes to the membrane of secretory vesicles that primarily carry TGFβ1 and binds to microtubules, thereby tethering secretory vesicles to microtubules and transporting them to the cell periphery as the marginal band develops.