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3D Printing in Nephrology

発表形態:
著書
主要業績:
主要業績
単著・共著:
分担執筆の共著
発表年月:
2022年10月
DOI:
10.1007/978-3-031-11570-7_9
会議属性:
指定なし
査読:
有り
リンク情報:

日本語フィールド

著者:
Nonaka T, Nagaishi Y, Murata D, Hara H, Nakayama K
題名:
3D Printing in Nephrology
発表情報:
Innovations in Nephrology ページ: 141–156
キーワード:
Tissue engineering, Bio-3D printing, Kidney biofabrication, Kidney organoid, Urine excretion pathway Decellularization, Kenzan method
概要:
Renal replacement therapy is currently limited to dialysis and renal transplantation, and the development of new technologies to regenerate kidney function is being pursued. Bioengineered tissue regeneration can now produce three-dimensional (3D) structures, and bio-3D printing technology, a revolutionary advancement, has given hope to creating cell-derived kidney tissue. Bioprinting the entire functional kidney has not been completed, but some studies have done so with a portion of the nephron. Embryonic stem cells or induced pluripotent stem cell-derived kidney organoids have been generated, which functionally mature after transplantation. Kidney decellularization induces the urine excretion pathway, and the Kenzan method is anticipated to develop regenerative kidney medicine. Although there are many challenges in producing kidneys, combining these methods is expected to create transplantable kidneys for humans in the future.
抄録:

英語フィールド

Author:
Nonaka T, Nagaishi Y, Murata D, Hara H, Nakayama K
Title:
3D Printing in Nephrology
Announcement information:
Innovations in Nephrology Page: 141–156
Keyword:
Tissue engineering, Bio-3D printing, Kidney biofabrication, Kidney organoid, Urine excretion pathway Decellularization, Kenzan method
An abstract:
Renal replacement therapy is currently limited to dialysis and renal transplantation, and the development of new technologies to regenerate kidney function is being pursued. Bioengineered tissue regeneration can now produce three-dimensional (3D) structures, and bio-3D printing technology, a revolutionary advancement, has given hope to creating cell-derived kidney tissue. Bioprinting the entire functional kidney has not been completed, but some studies have done so with a portion of the nephron. Embryonic stem cells or induced pluripotent stem cell-derived kidney organoids have been generated, which functionally mature after transplantation. Kidney decellularization induces the urine excretion pathway, and the Kenzan method is anticipated to develop regenerative kidney medicine. Although there are many challenges in producing kidneys, combining these methods is expected to create transplantable kidneys for humans in the future.


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