The Tissue Bank of the Upper Austrian Red Cross in Linz, Austria, is a multi-tissue bank, processing corneal transplants (for PKP, for DMEK, pre-cut DMEK), homografts (aortic valve, pulmonary valve, pulmonal patch), amnion grafts (frozen or cryopreserved), autologous tissues and cells (ovarian tissue, cranial bone, PBSC) as well as investigational medicinal products and ATMPs (Aposec, APN401).This presentation sums up retrospective data of the endothelial cell count of corneae at the time of first evaluation and at the time of reevaluation before transplantation as well as the cell count of pre-cut DMEK before transplantation.Regarding corneal grafts it is advisable to review the data of the previous years to find potential factors influencing the cell count of corneal tissue. Certain factors as donor age or duration of time between death of the donor until the cornea is cultivated might have an impact on endothelial cell loss.719 corneal transplants were included in this data comparison (PKPs, Corneae for DMEK and pre-cut DMEK), which were evaluated between January 2017 and March 2021. The average donor age was 66 years (22 to 88yrs). The average time until enucleation was 18 hours after death (3 to 44h). The mean duration of cultivating the cornea until reevaluation before transplantation was 15 days (7 to 29d).The average cell count at time of first evaluation was 2723 c/mm² (1550 to 3950c/mm²), at the time of reevaluation before transplantation 2613c/mm² (1650 to 3325c/mm²) and of the pre-cut DMEK transplants 2550c/mm² (2000 to 3233c/mm²).The results show an average cell loss of 6% from time of first evaluation compared to the time of reevaluation before transplantation and an average cell loss of 9% for pre-cut DMEK in comparison to the cell count at first evaluation. Dividing the donors in age groups of 10 years shows no noticeable difference in the results as the cell count at first evaluation compared to reevaluation shows cell loss between 4,9% and 8,8% with no tendency of increasing cell loss regarding donor age. The same seems to be the case regarding duration of cultivation until reevaluation.The aim of the data review was to determine the cell loss of corneal transplants and attempt to identify possible factors having an impact on endothelial cell loss of cultivated corneae. In conclusion the data comparison shows that donor age and time of cultivation seem to have no impact on cell loss.
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http://dx.doi.org/10.1136/bmjophth-2022-EEBA.35 | DOI Listing |
ISME J
January 2025
HADAL & Nordcee, Department of Biology, University of Southern Denmark, Odense, Denmark.
Auxiliary metabolic genes encoded by bacteriophages can influence host metabolic function during infection. In temperate phages, auxiliary metabolic genes may increase host fitness when integrated as prophages into the host genome. However, little is known about the contribution of prophage-encoded auxiliary metabolic genes to host metabolic properties.
View Article and Find Full Text PDFAppl Biochem Biotechnol
January 2025
Department of Neurosurgery, General Medical 300 Hospital, No. 420 Huanghe Road, Guiyang City, 550006, Guizhou Province, China.
Spinal cord injury (SCI) is one of the devastating neurological disorders that leads to a loss of motor and sensory functions. Long non-coding RNA small nucleolar RNA host gene 6 (lncRNA SNHG6) plays a crucial role in inflammatory regulation across various diseases. This study investigates the role of SNHG6 in SCI development and its underlying regulatory mechanisms.
View Article and Find Full Text PDFBiogerontology
January 2025
Department of Histology and Embryology, Akdeniz University School of Medicine, Campus, 07070, Antalya, Türkiye.
Spermatogenesis is finely regulated by histone methylation, which is crucial for regulating gene expression and chromatin remodeling. Functional studies have demonstrated that the histone lysine methyltransferases (KMTs) SETD1B, CFP1, SETDB1, G9A, and SETD2 play pivotal roles in spermatogenesis through establishing the key histone methylation marks, H3K4me3, H3K9me2, H3K9me3, and H3K36me3, respectively. This study aimed to evaluate the spatiotemporal expression of these KMTs and methylation marks as well as senescence-associated β-galactosidase (β-GAL), transcriptional activity, and apoptosis rates in mouse testes during biological aging.
View Article and Find Full Text PDFBrain Struct Funct
January 2025
Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Zagreb, Croatia.
In this study, we analyzed the spatio-temporal pattern of expression of specific transcription factors (PITX2, FOXA1, BARHL1, FOXP1, FOXP2) in the human fetal subthalamic nucleus and its neighboring structures from 11 postconceptional weeks (PCW) to 3 postnatal months. We found that all analyzed transcription factors are expressed already during the early fetal period (at 11 PCW). Both FOXP1- and FOXP2-immunoreactive cells were found in the subthalamic nucleus as well as in the striatum, thalamus, reticular nucleus, but not in the zona incerta.
View Article and Find Full Text PDFFASEB J
January 2025
Laboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe, Japan.
DFNA1 (deafness, nonsyndromic autosomal dominant 1), initially identified as nonsyndromic sensorineural hearing loss, has been associated with an additional symptom: macrothrombocytopenia. However, the timing of the onset of hearing loss (HL) and thrombocytopenia has not been investigated, leaving it unclear which occurs earlier. Here, we generated a knock-in (KI) DFNA1 mouse model, diaphanous-related formin 1 (DIA1), in which Aequorea coerulescens green fluorescent protein (AcGFP)-tagged human DIA1(p.
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