Evidence map›Paper›PMID 41132337›Full record

ArticleTranslational andrology and urology2025

Decellularized rat tubules for tissue engineering.

Qianfeng Jia, Kailin Li, Tongyan Liu, Feng Kong, Shengtian Zhao, Xianzhen Yang, Yong Guan

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qianfeng Jia *Department of Urology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, China.
Kailin Li *First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Tongyan LiuDepartment of Ultrasound, The Second Hospital of Shandong University, Jinan, China.
Feng KongDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Shengtian ZhaoFirst Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Xianzhen YangDepartment of Urology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.
Yong GuanDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic kidney disease (CKD) remains a global health challenge, with tissue engineering strategies like decellularized scaffolds offering potential solutions for functional renal regeneration, yet hindered by the complexity of whole-organ recellularization. Since the recellularization process is limited in whole organs, we propose to decellularize renal tubules and assess whether they exhibit enhanced recellularization potential, thereby offering a novel strategy for kidney regeneration. Methods: This study presents a microscale approach utilizing decellularized rat renal tubules to address these limitations. Renal tubules were microdissected from rat kidneys and then subjected to decellularization treatment with 0.5% sodium dodecyl sulfate (SDS) for 2 minutes. The decellularized renal tubules were structurally and compositionally characterized through immunofluorescence, transmission electron microscopy (TEM), DNA quantification, and collagen IV enzyme-linked immunosorbent assay (ELISA). Results: We successfully obtained decellularized renal tubule scaffolds, in which cellular components were removed while tubular basement membranes and extracellular matrix (ECM) architecture were preserved. TEM confirmed the ultrastructural integrity. Conclusions: The most significant contribution of this work is the establishment of a reproducible method for generating acellular renal tubule scaffolds that retain native ECM properties, providing a critical platform for studying cell-ECM interactions, disease modeling, and drug screening, thereby advancing targeted renal tissue engineering applications.

Indexed as

chronic kidney disease (CKD)Decellularizationextracellular matrix (ECM)renal tubuletissue engineering

Identifiers

PMID41132337
PMCPMC12541505

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.