Experimental strategies to improve in vitro models of renal ischemia
Abstract
Ischemia has elicited a great deal of interest among the scientific community due to its role in life-threatening pathologies such as cancer, stroke, acute renal failure, and myocardial infarction. Oxygen deprivation (hypoxia) associated with ischemia has recently become a subject of intense scrutiny. New investigators may find it challenging to induce hypoxic injury in vitro. Researchers may not always be aware of the experimental barriers that contribute to this phenomenon. Furthermore, ischemia is associated with other major insults, such as excess carbon dioxide (hypercapnia), nutrient deprivation, and accumulation of cellular wastes. Ideally, these conditions should also be incorporated into in vitro models. Therefore, the motivation behind this review is to: i. delineate major in vivo ischemic insults; ii. identify and explain critical in vitro parameters that need to be considered when simulating ischemic pathologies; iii. provide recommendations to improve experiments; and as a result, iv. enhance the validity of in vitro results for understanding clinical ischemic pathologies. Undoubtedly, it is not possible to completely replicate the in vivo environment in an ex vivo model system. In fact, the primary goal of many in vitro studies is to elucidate the role of specific stimuli during in vivo pathological events. This review will present methodologies that may be implemented to improve the applicability of in vitro models for understanding the complex pathological mec…
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In vitro systems allow precise control of conditions such as oxygen levels and medium perfusion.
“in vitro systems allow precise control of conditions such as oxygen levels and medium perfusion”
From Material-dependent oxygen transport governs ischemia-reperfusion injury and drug response in a kidney microphysiological system (2026) · cites this paper as Russ et al., 2007
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HIF-1: mediator of physiological and pathophysiological responses to hypoxia
Semenza, G. L. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.4.1474 · Cited by 1,822 · see citing works
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Kutsuzawa, N., Nakamura, H., Shinha, K., & Kimura, H. (2026) · Frontiers in Toxicology · doi:10.3389/ftox.2026.1854389
- Authors
- Russ, A. L., Haberstroh, K. M., & Rundell, A. E.
- Affiliations
- Purdue University West Lafayette (US)
- Brown University (US)
- Corresponding author
- Rundell, Ann E.
- ORCID
- Russ, Alissa L.
- Venue
- Experimental and Molecular Pathology
- Publisher
- Elsevier BV
- Published
- 2007-10
- Volume
- 83
- Issue
- 2
- Pages
- 143-159
- ISSN
- 0014-4800 (ISSN-L)
- OpenAlex
- W2049016339
- Cited by
- 34
- References
- 1
- Citations by year
- 2026: 1 · 2025: 1 · 2021: 3 · 2020: 2 · 2018: 2 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 4 · 2012: 3
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental and Molecular Pathology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
- Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Keywords
- renal ischemia, hypoxia, in vitro model, oxygen deprivation, hypercapnia, nutrient deprivation, model validity, ex vivo model, acute kidney injury
- MeSH terms
- Humans, Hypercapnia, Ischemia, Kidney Diseases, Kidney Medulla, Kidney Tubules, Proximal, Renal Circulation, Cell Hypoxia, Urothelium
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