Evidence map›Paper›PMID 39478629›Full record

ArticleHistology and histopathology2025

Does old-to-young kidney transplantation rejuvenate old donor kidneys?

Mayumi Takahashi-Kobayashi, Kunio Kawanishi, Joichi Usui, Satoshi Yamazaki, Surya V Seshan, Kunihiro Yamagata

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Article in Histology and histopathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Mayumi Takahashi-KobayashiDepartment of Nephrology, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Kunio KawanishiDepartment of Experimental Pathology, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Joichi UsuiDepartment of Nephrology, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan. j-usui@md.tsukuba.ac.jp.
Satoshi YamazakiLaboratory of Stem Cell Therapy, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Surya V SeshanDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Kunihiro YamagataDepartment of Nephrology, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.

Funding

Japan Society for the Promotion of Science (JSPS) KAKENHI JP19KK0216Japan Society for the Promotion of Science (JSPS) KAKENHI JP21H02822Japan Society for the Promotion of Science (JSPS) KAKENHI JP22KJ0426Japan Society for the Promotion of Science (JSPS) KAKENHI JP23K18308JST START University Promotion Type JPMJST2052
6 · The paper itself

Abstract

backgroundThe number of older organ donors is increasing due to the aging population. Aged kidneys often face problems such as delayed graft function but previous murine experiments suggested the possibilities of rejuvenation, for example, in a parabiosis setting between old and young mice. To investigate kidney-graft rejuvenation, we compared an old-to-young (O-Y) patient transplantation group and a transplantation group with donors/recipients of approx. the same age (SA) with the renal senescence marker p16 in kidney biopsy samples at baseline and one year post-transplantation.

methodsWe retrospectively analyzed our hospital's 32 cases of living-donor ABO-compatible transplants performed between 2013-2020. Both the baseline and one-year biopsy (n=9) or only the baseline biopsy (n=32) were analyzed. We divided the nine cases into an O-Y group (donors' median age 68 yrs, recipients 41, difference -27) and an SA group (donors' median age 53 yrs, recipients 51.5, difference -3.5). p16 was stained with the clones JC8 and E6H4 to determine the precise p16-positive rate.

resultsThe 32 baseline biopsies' p16-positive rate was weakly related to donor age, suggesting that the p16-positive rate can help evaluate kidney senescence. The (n=5) O-Y group's p16-positive rates were at baseline 0.08 and one year 0.12; the (n=4) SA group's rate was 0.03 at both baseline and one year.

conclusionsNo kidney rejuvenation was observed, even when old donor kidneys went to young recipients.

Indexed as

AgingKidneyKidney TransplantationRejuvenationAdultAgedAge FactorsCyclin-Dependent Kinase Inhibitor p16FemaleGraft SurvivalHumansLiving DonorsMaleMiddle AgedRetrospective StudiesTissue DonorsCyclin-Dependent Kinase Inhibitor p16

Identifiers

PMID39478629

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.