U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

SRX20641633: GSM7469531: hippocampi, oxygen, 6h, rep1; Callithrix jacchus; RNA-Seq
4 ILLUMINA (Illumina NovaSeq 6000) runs: 370.3M spots, 111.1G bases, 40.2Gb downloads

External Id: GSM7469531_r1
Submitted by: Department of Anesthesiology, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Study: Sevoflurane increases FKBP5 expression in microglia in the brains of aged marmosets and mice
show Abstracthide Abstract
Background: Inhalation anesthetics may trigger the hypothalamic–pituitary–adrenal (HPA) axis. FK-506 binding protein (FKBP5) is a critical factor that regulates the HPA axis and is associated with perioperative neurocognitive impairment. However, it is unclear how inhalation anesthetics affects the expression of FKBP5 in different neural cells in the brain. Methods: We used single-nucleus RNA sequencing to characterize hippocampal transcriptome profiles in the brains of aged marmosets and mice after sevoflurane anesthesia. Results: Higher levels of FKBP5 were found in the hippocampi of aged mice after sevoflurane anesthesia. Single nuclear RNA sequencing results from aged mice and marmosets showed that the increased expression of FKBP5 mainly occurred in microglia. The expression of FKBP5 in the hippocampi of aged marmosets and mice increased following long-term exposure to sevoflurane anesthesia. Additionally, the brains of these animals displayed a marked increase in the expression of FKBP5 in microglia after sevoflurane anesthesia. Conclusion: Long-term exposure to sevoflurane augments FKBP5 expression in the hippocampi of aged marmosets and mice, specifically in the microglia. Overall design: Control and sevoflurane anesthetized hippocampi of aged mice and aged marmosets
Sample: hippocampi, oxygen, 6h, rep1
SAMN35677763 • SRS17940497 • All experiments • All runs
Library:
Name: GSM7469531
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Each sample was placed in a sterile Petri dish on ice. Fat, fibrous and necrotic areas were removed, and the tissue was subsequently minced to smaller pieces of less than 3 mm. Samples were first washed with phosphate-buffered saline (PBS), minced into small pieces (approximately 1mm3) on ice and enzymatically digested with collagenase Ⅱ (Worthington) for 60 min at 37°C, with agitation. Subsequently, the sample was filtered using a 70-mm nylon mesh (Miltenyi #130-095-823). 10 ml of this cell suspension was counted by Trypan Blue to determine the concentration of live cells. The sample was then centrifuged at 300g and 4℃ for 5 min, and the supernatant was discarded. The cell pellet was resuspended in 1 ml freezing media (Gibco) for long term cryopreservation in liquid nitrogen. Throughout the dissociation procedure, cells were maintained on ice whenever possible, and the entire procedure was completed in less than 1 hr. Cryopreserved single-cell suspensions were promptly thawed and prepared as outlined by the 10x Genomics Single Cell 3 v3.1 Reagent Kit user guide.
Runs: 4 runs, 370.3M spots, 111.1G bases, 40.2Gb
Run# of Spots# of BasesSizePublished
SRR2487792499,243,38129.8G10.8Gb2024-10-30
SRR2487792576,455,44722.9G8.3Gb2024-10-30
SRR2487792690,799,70727.2G9.8Gb2024-10-30
SRR24877927103,767,74231.1G11.2Gb2024-10-30

ID:
28070558

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...