# Translational Potential: Kidney Tubuloids in Precision Medicine and Regenerative Nephrology

**Authors:** Muhammad Kamal Hossain, Hwa-Young Lee, Hyung-Ryong Kim

PMC · DOI: 10.3390/pharmaceutics18020147 · 2026-01-23

## TL;DR

Kidney tubuloids offer a promising platform for modeling kidney diseases and testing treatments with greater accuracy than traditional models.

## Contribution

This paper highlights recent advances in tubuloid technologies and proposes a roadmap for their clinical translation in precision nephrology.

## Key findings

- Tubuloids provide stable, reproducible cultures enriched for functional tubular cells.
- They enable high-fidelity modeling of tubular disorders and nephrotoxicity.
- Integration with microfluidics and gene-editing enhances their physiological realism.

## Abstract

Advances in kidney organoid technologies have expanded opportunities to model human renal development, disease, and therapeutic response. Yet pluripotent stem cell-derived organoids remain limited by cellular heterogeneity, incomplete tubular maturation and low scalability, restricting their translational relevance. Tubular-specific organoids, derived from adult kidney epithelium, address many of these constraints by providing stable, reproducible cultures enriched for functional proximal and distal tubular cells. Their polarized transport, metabolic activity and patient-specific phenotypes enable high-fidelity modeling of acute and chronic tubular disorders, nephrotoxicity, and inherited tubulopathies—areas where conventional animal and cell-line models often fall short. In this Perspective, we outline recent advances that position tubuloids as a versatile platform for drug screening, toxicity testing and personalized disease modeling. We highlight emerging integration with microfluidics, biomaterials, and gene-editing strategies that promise greater physiological realism and precision therapeutics. We also discuss persistent barriers that impede broader adoption and clinical translation. We propose a roadmap for advancing tubuloid technologies toward precision nephrology and their future incorporation into diagnostic, pharmacological and regenerative pipelines.

## Full-text entities

- **Genes:** CD24 (CD24 molecule) [NCBI Gene 100133941] {aka CD24A}, PKD2 (polycystin 2, transient receptor potential cation channel) [NCBI Gene 5311] {aka APKD2, PC2, PKD4, Pc-2, TRPP2}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, SLC12A3 (solute carrier family 12 member 3) [NCBI Gene 6559] {aka NCC, NCCT, TSC}, NOG (noggin) [NCBI Gene 9241] {aka SYM1, SYNS1, SYNS1A}, SLC12A1 (solute carrier family 12 member 1) [NCBI Gene 6557] {aka BSC, BSC-1, BSC1, CCC2, NKCC2}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SLC9A3 (solute carrier family 9 member A3) [NCBI Gene 6550] {aka DIAR8, NHE-3, NHE3}, CLU (clusterin) [NCBI Gene 1191] {aka AAG4, APO-J, APOJ, CLI, CLU1, CLU2}, KL (klotho) [NCBI Gene 9365] {aka HFTC3, KLA}, POU2F2 (POU class 2 homeobox 2) [NCBI Gene 5452] {aka OCT2, OTF2, Oct-2}, Scnn1a (sodium channel, nonvoltage-gated 1 alpha) [NCBI Gene 20276] {aka ENaC, SCNEA, Scnn1, mENaC}, Aqp3 (aquaporin 3) [NCBI Gene 11828] {aka AQP-2}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, AQP1 (aquaporin 1 (Colton blood group)) [NCBI Gene 358] {aka AQP-CHIP, CHIP28, CO}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, SLC47A1 (solute carrier family 47 member 1) [NCBI Gene 55244] {aka MATE1}, HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}, WT1 (WT1 transcription factor) [NCBI Gene 7490] {aka AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1}, CLCNKB (chloride voltage-gated channel Kb) [NCBI Gene 1188] {aka CLCKB, ClC-K2, ClC-Kb}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, Aqp2 (aquaporin 2) [NCBI Gene 11827] {aka AQP-CD, WCH-CD, cph, jpk}, VIM (vimentin) [NCBI Gene 7431], SPP1 (secreted phosphoprotein 1) [NCBI Gene 6696] {aka BNSP, BSPI, ETA-1, OPN}, ABCC2 (ATP binding cassette subfamily C member 2) [NCBI Gene 1244] {aka ABC30, CMOAT, DJS, MRP2, cMRP}, PKD1 (polycystin 1, transient receptor potential channel interacting) [NCBI Gene 5310] {aka PBP, PC1, Pc-1, TRPP1, eliosin}, LCN2 (lipocalin 2) [NCBI Gene 3934] {aka 24p3, MSFI, NGAL, p25}, KCNK3 (potassium two pore domain channel subfamily K member 3) [NCBI Gene 3777] {aka DDSA, K2p3.1, OAT1, PPH4, TASK, TASK-1}, HAVCR1 (hepatitis A virus cellular receptor 1) [NCBI Gene 26762] {aka CD365, HAVCR, HAVCR-1, KIM-1, KIM1, TIM}, NPHS1 (NPHS1 adhesion molecule, nephrin) [NCBI Gene 4868] {aka CNF, NPHN, nephrin}, Avpr2 (arginine vasopressin receptor 2) [NCBI Gene 12000] {aka ADHR, DI1, DIR, ND1, V2R, VPV2R}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, BMP7 (bone morphogenetic protein 7) [NCBI Gene 655] {aka OP-1}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}
- **Diseases:** Bartter and Gitelman syndromes (MESH:D053579), cystic kidney diseases (MESH:D052177), nephrotoxic compounds (MESH:D005597), tubular transport defects (MESH:D015499), toxic injuries (MESH:D064420), acute and chronic tubular disorders (MESH:D040701), nephrogenic diabetes insipidus (MESH:D018500), drug nephrotoxicity (MESH:D000081015), kidney disease (MESH:D007674), cyst (MESH:D003560), ADPKD (MESH:D016891), polycystic kidney disease (MESH:D007690), transport disorders (MESH:D007706), mitochondrial dysfunction (MESH:D028361), inflammation (MESH:D007249), monogenic disease (MESH:D004194), injury (MESH:D014947), fibrosis (MESH:D005355), congenital anomalies (MESH:D000013), cystic fibrosis (MESH:D003550), swelling (MESH:D004487), CKD (MESH:D051436), tubular injury (MESH:D000230), congenital tubulopathies (MESH:C557674), AKI (MESH:D058186), monogenic disorders (MESH:D009358), hypoxia (MESH:D000860), inherited tubulopathies (MESH:D030342)
- **Chemicals:** doxorubicin (MESH:D004317), cyclosporin A (MESH:D016572), puromycin (MESH:D011691), sodium (MESH:D012964), Cisplatin (MESH:D002945), gammaH2AX (-), curcumin (MESH:D003474), rifampicin (MESH:D012293), forskolin (MESH:D005576), lipids (MESH:D008055), ATP (MESH:D000255), glucose (MESH:D005947), amiloride (MESH:D000584), tolvaptan (MESH:D000077602), tenofovir (MESH:D000068698), oxygen (MESH:D010100), water (MESH:D014867), electrolyte (MESH:D004573), luminal (MESH:D010634), citrinin (MESH:D002953), Gentamicin (MESH:D005839)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944275/full.md

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Source: https://tomesphere.com/paper/PMC12944275