Chie Kise

Dr. Chie Kise


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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11 December 2024 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
YSYuka Sasaki
Yuka Sasaki
TITakuma Inouchi
Takuma Inouchi
CKChie Kise
Chie Kise
RNRyusuke Nakatsuka
Ryusuke Nakatsuka
AIAmane Inoue
Amane Inoue
TNTadashige Nozaki
Tadashige Nozaki

11 July 2026 in Cells
Verified
Journal Article
Open access
PDF file
CKChie Kise
Chie Kise
RNRyusuke Nakatsuka
Ryusuke Nakatsuka
AKAkiyo Kawamoto
Akiyo Kawamoto
YSYuka Sasaki
Yuka Sasaki
HHHirofumi Hitomi
Hirofumi Hitomi
TNTadashige Nozaki
Tadashige Nozaki
Several protocols have been reported for inducing parathyroid differentiation from human pluripotent stem cells in vitro. However, the efficiency of terminal differentiation into mature parathyroid cells remains limited. In this study, we performed comparative transcriptomic analyses of parathyroid lineage-induced human induced pluripotent stem (iPS) cells to clarify their developmental stage identity. Comparative analyses with adult parathyroid adenoma, used as a surrogate reference for mature parathyroid cells, and thymuses revealed that the differentiated cells exhibited gene expression patterns consistent with early-stage parathyroid and thymus development, including TBX1, which is required for fate determination of the parathyroid–thymic primordium. On the other hand, the expression of mature parathyroid marker genes, such as PTH, GCM2, and the calcium-sensing receptor (CaSR), remained markedly lower than that in parathyroid adenoma. Under the differentiation conditions and durations examined, application of modified differentiation protocols did not significantly enhance the expression of mature parathyroid markers, although pharyngeal pouch developmental gene expression was maintained. Our findings indicate that current in vitro differentiation systems effectively induce the parathyroid–thymic primordium stage, while a developmental bottleneck at the transition from the primordium toward parathyroid lineage commitment remains.