Projects / Programmes
Development of advanced multidimensional in vitro kidney models
Code |
Science |
Field |
Subfield |
3.06.00 |
Medical sciences |
Cardiovascular system |
|
Code |
Science |
Field |
3.02 |
Medical and Health Sciences |
Clinical medicine |
isolation of novel cell lines, characterization of novel cell lines, testing of novel cell lines, in vitro kidney models
Data for the last 5 years (citations for the last 10 years) on
October 15, 2025;
Data for score A3 calculation refer to period
2020-2024
Data for ARIS tenders (
04.04.2019 – Programme tender,
archive
)
Database |
Linked records |
Citations |
Pure citations |
Average pure citations |
WoS |
876
|
52,926
|
51,107
|
58.34
|
Scopus |
793
|
61,158
|
59,262
|
74.73
|
Organisations (4)
, Researchers (27)
0334 University Medical Centre Maribor
no. |
Code |
Name and surname |
Research area |
Role |
Period |
No. of publicationsNo. of publications |
1. |
27593 |
PhD Sebastjan Bevc |
Cardiovascular system |
Head |
2022 - 2025 |
852 |
2. |
23190 |
Benjamin Dvoršak |
Cardiovascular system |
Researcher |
2022 - 2025 |
112 |
3. |
23191 |
PhD Robert Ekart |
Cardiovascular system |
Researcher |
2022 - 2025 |
705 |
4. |
15751 |
PhD Radovan Hojs |
Metabolic and hormonal disorders |
Researcher |
2022 - 2025 |
816 |
5. |
30461 |
PhD Eva Jakopin |
Metabolic and hormonal disorders |
Researcher |
2022 - 2025 |
95 |
6. |
30464 |
PhD Maša Knehtl |
Metabolic and hormonal disorders |
Researcher |
2022 - 2025 |
126 |
7. |
52585 |
Tadej Petreski |
Cardiovascular system |
Researcher |
2022 - 2025 |
142 |
8. |
52577 |
PhD Nejc Piko |
Cardiovascular system |
Researcher |
2022 - 2025 |
148 |
9. |
57784 |
Luka Varda |
Cardiovascular system |
Researcher |
2023 - 2025 |
53 |
10. |
36118 |
PhD Nina Vodošek Hojs |
Metabolic and hormonal disorders |
Researcher |
2022 - 2025 |
151 |
0381 University of Ljubljana, Faculty of Medicine
no. |
Code |
Name and surname |
Research area |
Role |
Period |
No. of publicationsNo. of publications |
1. |
22462 |
PhD Nika Kojc |
Oncology |
Researcher |
2022 - 2025 |
208 |
2. |
36130 |
Jerica Pleško |
|
Technical associate |
2022 - 2025 |
38 |
2334 University of Maribor, Faculty of Medicine
2841 General Hospital Murska Sobota
no. |
Code |
Name and surname |
Research area |
Role |
Period |
No. of publicationsNo. of publications |
1. |
55479 |
Nino Cmor |
Cardiovascular system |
Researcher |
2022 - 2025 |
11 |
2. |
55480 |
Eva Dora |
Cardiovascular system |
Researcher |
2022 - 2025 |
15 |
3. |
30713 |
PhD Jerneja Farkaš-Lainščak |
Medical sciences |
Researcher |
2022 - 2025 |
441 |
4. |
22680 |
PhD Mitja Lainščak |
Cardiovascular system |
Researcher |
2022 - 2025 |
749 |
Abstract
The kidney is a complex organ composed mainly of glomerular, tubular, mesangial cells, podocytes, and endothelial cells. The fact that renal cells are terminally differentiated at 34 weeks of gestation is the main obstacle in the regeneration and treatment of acute or chronic renal damage. Considering the annually increasing number of patients with chronic kidney disease, related research aims to improve existing and develop new renal replacement therapy methods. Besides, given the increasing polypharmacy in the ever-ageing population, consideration should be given to developing new drug safety testing methods (e.g., advanced nephrotoxicity models, drug excretion and related interactions). One possible way to address these issues is to isolate and culture renal cells to produce functional in vitro models. The more successful such mimicry is regarding native tissue, the higher is their prediction potential in the systematic investigation of acute and chronic kidney disease's pathophysiology and/or testing of complex drug-related pharmacokinetic aspects. In this proposal, we have chosen such a path.
Our project aims to develop 2D and 3D functional in vitro kidney models to study acute and chronic kidney pathophysiology. The developed models will be based on our own isolated kidney cells from kidney (punch-based) biopsy tissue samples of non-cancerous patients. More specifically, the developed in vitro cell models will aim:
1) for excretion observation and nephrotoxicity studies (2D models will focus on the “E part” of the ADME system of non-clinical testing, as well as enable testing of potential drug toxicities towards kidney tissue),
2) to try to recapitulate the complexity of nephron, enabling systematic studies of kidney disease pathologies (3D models will focus on partial and/or full kidney failure).
Our research is divided into several work packages, where each chapter represents an upgraded level of complexity of the developed in vitro models in previous chapters. The final step will comprise developing and testing functional 3D bioprinted or spheroid models of kidney failure.