Lack of Neuroprotection with a Single Intravenous Infusion of Human Amnion Epithelial Cells after Severe Hypoxia–Ischemia in Near-Term Fetal Sheep

• Published in: International journal of molecular sciences Vol. 23; no. 15; p. 8393
• Main Authors: Davidson, Joanne O., van den Heuij, Lotte G., Dhillon, Simerdeep K., Miller, Suzanne L., Lim, Rebecca, Jenkin, Graham, Gunn, Alistair J., Bennet, Laura
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.08.2022; MDPI
• Subjects: Amnion; Apoptosis; Brain damage; Brain injury; Disability; EEG; Electroencephalography; Encephalopathy; Epithelial cells; Epithelium; Experiments; fetal sheep; Fetuses; human amnion epithelial cells; Hypoxia; hypoxia ischemia; Inflammation; Injury prevention; Intravenous administration; Intravenous infusion; Ischemia; Neostriatum; Neuroprotection; Oligodendrocytes; Sheep; Stem cells; Substantia alba; Thalamus; Umbilical cord
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23158393

Background: Hypoxic–ischemic encephalopathy (HIE) around the time of birth results from loss of oxygen (hypoxia) and blood supply (ischemia). Exogenous infusion of multi-potential cells, including human amnion epithelial cells (hAECs), can reduce hypoxic–ischemic (HI) brain injury. However, there are few data on treatment of severe HI in large animal paradigms at term. The aim of the current study was to determine whether infusion of hAECs early after injury may reduce brain damage after ischemia in near-term fetal sheep. Methods: Chronically instrumented fetal sheep (0.85 gestation) received 30 min of global cerebral ischemia followed by intravenous infusion of hAECs from 2 h after the end of ischemia (ischemia-hAEC, n = 6) or saline (ischemia-vehicle, n = 7). Sham control animals received sham ischemia with vehicle infusion (sham control, n = 8). Results: Ischemia was associated with significant suppression of EEG power and spectral edge frequency until the end of the experiment and a secondary rise in cortical impedance from 24 to 72 h, which were not attenuated by hAEC administration. Ischemia was associated with loss of neurons in the cortex, thalamus, striatum and hippocampus, loss of white matter oligodendrocytes and increased microglial numbers in the white matter, which were not affected by hAEC infusion. Conclusions: A single intravenous administration of hAECs did not reduce electrographic or histological brain damage after 30 min of global cerebral ischemia in near-term fetal sheep.