Takahiro Kikawada
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Recent Grants
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Elucidation of anhydrobiosis in Triops longicaudatus
Open Date: 2022-04-22
Close Date: 2024-03-31
Grant: Close
Genome protection and repair mechanisms for the extreme desiccation tolerance, anhydrobiosis
Open Date: 2022-04-01
Close Date: 2026-03-31
Grant: Close
Preservation of mammalian genetic resources and study for the developmental mechanism using freeze-dried cells
Open Date: 2018-04-01
Close Date: 2023-03-31
Grant: Close
Studies on cryopreservation mechanism of intracellular trehalose introduced through trehalose transporter
Open Date: 2017-06-30
Close Date: 2019-03-31
Grant: Close
Gene regulatory networks underlying 3-D conformational change in genome associated with anhydrobiosis
Open Date: 2017-04-01
Close Date: 2021-03-31
Articles (11)
Pv11 is the only animal cell line that, when preconditioned with a high concentration of trehalose, can be preserved in the dry state at room temperature for more than one year while retaining the ability to resume proliferation. This extreme desiccation tolerance is referred to as anhydrobiosis. Here, we identified a transporter that contributes to the recovery of Pv11 cells from anhydrobiosis. In general, the solute carrier 5 (SLC5)-type secondary active transporters cotransport Na + and carbohydrates including glucose. The heterologous expression systems showed that the transporter belonging to the SLC5 family, whose expression increases upon rehydration, exhibits Na + -dependent trehalose transport activity. Therefore, we named it STRT1 (sodium-ion trehalose transporter 1). We report an SLC5 family member that transports a naturally occurring disaccharide, such as trehalose. Knockout of the Strt1 gene significantly reduced the viability of Pv11 cells upon rehydration after desiccation. During rehydration, when intracellular trehalose is no longer needed, Strt1 -knockout cells released the disaccharide more slowly than the parental cell line. During rehydration, Pv11 cells became roughly spherical due to osmotic pressure changes, but then returned to their original spindle shape after about 30 min. Strt1 -knockout cells, however, required about 50 min to adopt their normal morphology. STRT1 probably regulates intracellular osmolality by releasing unwanted intracellular trehalose with Na + , thereby facilitating the recovery of normal cell morphology during rehydration. STRT1 likely improves the viability of dried Pv11 cells by rapidly alleviating the significant physical stresses that arise during rehydration.
Year:
2024
Year:
2023
Aphids harbor proteobacterial endosymbionts such as Buchnera aphidicola housed in specialized bacteriocytes derived from host cells. The endosymbiont Buchnera supplies essential amino acids such as arginine to the host cells and, in turn, obtains sugars needed for its survival from the hemolymph. The mechanism of sugar supply in aphid bacteriocytes has been rarely studied. It also remains unclear how Buchnera acquires its carbon source. The hemolymph sugars in Acyrthosiphon pisum are composed of the disaccharide trehalose containing two glucose molecules. Here, we report for the first time that trehalose is transported and used as a potential carbon source by Buchnera across the bacteriocyte plasma membrane via trehalose transporters. The current study characterized the bacteriocyte trehalose transporter Ap_ST11 (LOC100159441) using the Xenopus oocyte expression system. The Ap_ST11 transporter was found to be proton‐dependent with a K m value ≥700 mM. We re‐examined the hemolymph trehalose at 217.8 mM using a fluorescent trehalose sensor. The bacteriocytes did not obtain trehalose by facilitated diffusion along the gradient across cellular membranes. These findings suggest that trehalose influx into the bacteriocytes depends on the extracellular proton‐driven secondary electrochemical transporter.
Year:
2022
Year:
2022
Year:
2022
Year:
2022
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2022
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2022
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2021
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2021
Year:
2021
Collaborators (5)
Shingo Kikuta
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Michele Cesari
Associate Professor
University of Modena and Reggio Emilia
Richard CORNETTE
Chief Principal Researcher
Institute of Agrobiological Sciences, NARO
Oleg Gusev
Professor (Associate)
Juntendo University
Yugo Miyata
Tokyo Medical and Dental University
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