Cell division is an important and fundamental process which is contributed to cell proliferation and differentiation. For mammalian, female meiotic divisions are typically asymmetric, generating two kinds of daughter cells with unequal size. This mechanism is essential to retain sufficient storage material for the development of embryo after fertilization. In order to achieve asymmetric division, the most crucial procedure is the migration of spindle from the center to cortex in meiosis I. In this paper, we used a set of PDEs with two reacting and diffusing chemical morphogens and adding another substance to represent cortex actin to investigate the mechanism of spindle movement in meiosis I. According to our simulation result, our hypothesis showed good consistency with real division process.
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Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Kojo, Kei H.
Higaki, Takumi
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Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Higaki, Takumi
Kutsuna, Natsumaro
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Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Kutsuna, Natsumaro
Yoshida, Yuya
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Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Yoshida, Yuya
Yasuhara, Hiroki
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Kansai Univ, Fac Chem Mat & Bioengn, Dept Life Sci & Biotechnol, Suita, Osaka 5648680, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Yasuhara, Hiroki
Hasezawa, Seiichiro
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Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
Japan Sci & Technol Agcy JST, Adv Measurement & Anal, Chiyoda Ku, Tokyo 1028666, JapanUniv Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
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St Louis Univ, Sch Med, Dept Physiol & Pharmacol, Colin Flaveny Lab, St Louis, MO USASt Louis Univ, Sch Med, Dept Physiol & Pharmacol, Colin Flaveny Lab, St Louis, MO USA
Valfort, Aurore-Cecile
Launay, Caroline
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Lyon Univ, Univ Claude Bernard, ENS Lyon, UnivLyon,Lab Biol & Modelling Cell, Lyon, FranceSt Louis Univ, Sch Med, Dept Physiol & Pharmacol, Colin Flaveny Lab, St Louis, MO USA
Launay, Caroline
Semon, Marie
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Lyon Univ, Univ Claude Bernard, ENS Lyon, UnivLyon,Lab Biol & Modelling Cell, Lyon, FranceSt Louis Univ, Sch Med, Dept Physiol & Pharmacol, Colin Flaveny Lab, St Louis, MO USA
Semon, Marie
Delattre, Marie
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Lyon Univ, Univ Claude Bernard, ENS Lyon, UnivLyon,Lab Biol & Modelling Cell, Lyon, FranceSt Louis Univ, Sch Med, Dept Physiol & Pharmacol, Colin Flaveny Lab, St Louis, MO USA