OC 28.2 Neutrophil-Derived Factor XIII-A Transglutaminase Contributes to Adipose Tissue Fibrosis and Inflammation in Mouse-Obesity Model
Bibliographic record
Abstract
Background: Acute on chronic renal injury (ACRI) is a major health problem.Tubulointerstitial damage in diabetic kidney disease (DKD) impairs the outcome of acute kidney injury (AKI), possibly reflecting exhaustion of the renal regenerative capacity in DKD.The role of activated PC (aPC), which protects against DKD progression and reverses glucose-induced tubular senescence, for renal regeneration after AKI has not been elucidated hitherto.Aims: To delineate the possible role of aPC in controlling renal tubular cell proliferation and repair in DKD after AKI.Methods: A model of ACRI was established in mice with persistent hyperglycemia followed by ischemia-reperfusion injury (IRI).Control mice were compared to mice pre-treated with aPC.Lineage tracing and kidney single-cell RNA sequencing (scRNA-seq) were performed to identify the possible mechanisms of aPC.Ex-vivo analyses of mouse tissues and in vitro work were conducted to gain mechanistic insights.Results: DKD markedly aggravated histopathological changes and functional impairment following IRI.Pre-treatment with aPC conveyed renal protection.Lineage tracing studies revealed increased proliferation and expansion of tubular cell clones upon aPC pre-treatment.scRNA-seq showed marked changes in different cell populations in DKD mice subjected to IRI mainly in the tubular and immune cell clusters.Functional annotations identified activation of senescence pathways and inflammatory pathways in tubular cell and immune cell clusters, respectively.Pretreatment with aPC protected against these changes.Mechanistically, aPC treatment reduced oxidative DNA damage and induction of senescence in renal tubular cells, which was associated with increased proliferation and ex-vivo clonal expansion of tubular cells in DKD mice following IRI.Conclusion(s): aPC improves the outcome of ACRI by enhancing the regenerative capacity of renal tubular cells and reducing the inflammatory response.In DKD, aPC reverses glucose-induced senescence in tubular cells, thus restoring the regenerative capacity.Therefore, aPC-based therapeutics may provide innovative approaches to ACRI in patients with pre-existing DKD.
Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.
How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.001 | 0.001 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.001 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.001 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".