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Updated: Apr 23, 2026

Peroxisome Staining in Mammalian Cells Using Peroxisome-Specific Probes
Published on: December 19, 2025
Spatio-temporal expression of peroxisome proliferator-activated receptor α during human prenatal development
Katerina Cizkova1, Aneta Rajdova, Jiri Ehrmann
1Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Insights
Peroxisome proliferator-activated receptor α (PPARα) is expressed early in human prenatal development in the intestines, liver, and kidney. Its expression changes with organ development, offering insights into potential environmental impacts.
Area of Science:
- Developmental Biology
- Molecular Biology
- Toxicology
Background:
- Peroxisome proliferator-activated receptor α (PPARα) is a crucial transcription factor regulating metabolism and xenobiotic detoxification.
- Its role and expression patterns during human prenatal development remain largely uncharacterized.
- Understanding PPARα expression is vital for assessing the impact of environmental and pharmaceutical compounds on developing organisms.
Purpose of the Study:
- To investigate the spatio-temporal expression of PPARα in human embryonic and fetal intestines, liver, and kidney.
- To correlate PPARα expression patterns with the developmental stages and functional maturation of these organs.
- To establish a baseline for evaluating potential prenatal risks associated with PPARα-activating compounds.
Main Methods:
- Indirect two-step immunohistochemistry was employed.
- Human embryonic/fetal tissues (intestines, liver, kidney) were analyzed from the 5th to 20th week of intrauterine development (IUD).
- Expression patterns were examined in relation to developmental timing and anatomical structures.
Main Results:
- PPARα expression was detected early in prenatal development: 7th week (intestines), 5th week (liver), and 6th week (kidney).
- Age-dependent changes in PPARα expression were observed in the intestines and kidney, coinciding with organ functional onset.
- Specific changes included alterations along the intestinal crypt-villous axis (11th week IUD) and increased glomerular expression in the kidney (12th week IUD).
- Strong PPARα positivity was noted in developing blood elements within the liver.
Conclusions:
- PPARα is expressed early and dynamically throughout human prenatal development in key organs.
- Observed expression patterns suggest PPARα's involvement in organogenesis and functional maturation.
- This spatio-temporal expression data is foundational for assessing the prenatal effects of PPARα-ligand exposure.
Abstract:
Peroxisome proliferator-activated receptor α (PPARα) is a ligand-dependent transcription factor which is activated by various endogenous as well as exogenous compounds. It is involved in the regulation of a variety of biological processes, such as nutrient metabolism, energy homoeostasis, immunological response and xenobiotic metabolism. Little is known about its expression during human prenatal development. We examined the spatio-temporal expression pattern of PPARα in human embryonic/foetal intestines, liver and kidney from the 5th to 20th week of prenatal life by indirect two-step immunohistochemistry. PPARα expression can already be detected in the early stages of prenatal development; as early as the 7th week of intrauterine development (IUD) in the intestines, 5th week of IUD in the liver and 6th week of IUD in the kidney. We found age-dependent changes in the PPARα expression pattern in the intestines and kidney. These events occur approximately at the commencement of function of these organs. In the intestines, we detected an obvious change of the PPARα expression pattern along the crypt-villous axis in the 11th week of IUD. In the kidney, the most apparent change was increased expression of PPARα in glomeruli in the 12th week of IUD. Moreover, in the liver, we detected a strong positivity in part of the developing blood elements. Information about the spatio-temporal expression pattern of PPARα could be the first step in evaluating the potential harmful impact of a wide range of environmental or pharmaceutical compounds which serve as PPARα ligands on the developing human organism.
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