Literature DB >> 35245386

Small Molecule Signatures of Mice Lacking T-cell p38 Alternate Activation, a Model for Immunosuppression Conditions, after Total-Body Irradiation.

Evan L Pannkuk1,2, Evagelia C Laiakis1,2, Jerry Angdisen1, Meth M Jayatilake2, Pelagie Ake1, Lorreta Yun-Tien Lin1, Heng-Hong Li1,2, Albert J Fornace1,2.   

Abstract

Several diagnostic biodosimetry tools have been in development that may aid in radiological/nuclear emergency responses. Of these, correlating changes in non-invasive biofluid small-molecule signatures to tissue damage from ionizing radiation exposure show promise for inclusion in predictive biodosimetry models. Integral to dose reconstruction has been determining how genotypic variation in the general population will affect model performance. Here, we used a mouse model that lacks the T-cell receptor specific alternative p38 pathway [p38αβY323F, double knock-in (DKI) mice] to determine how attenuated autoimmune and inflammatory responses may affect dose reconstruction. We exposed adult male DKI mice (8-10 weeks old) to 2 and 7 Gy in parallel with wild-type mice and assessed perturbations in urine (days 1, 3, 7) and serum (day 1) using a global metabolomics approach. A multidimensional scaling plot showed excellent separation of radiation-exposed groups in wild-type mice with slightly dampened responses in DKI mice. Validated metabolite panels were developed for urine [N6,N6,N6-trimethyllysine (TML), N1-acetylspermidine, spermidine, carnitine, acylcarnitine C21H35NO5, aminohippuric acid] and serum [phenylalanine, glutamine, propionylcarnitine, lysophosphatidylcholine (LysoPC 14:0), LysoPC (22:5)] to determine the area under the receiver operating characteristic curve (AUROC). For both urine and serum, excellent sensitivity and specificity (AUROC > 0.90) was observed for 0 Gy vs. 7 Gy groups irrespective of genotype using identical metabolite panels. Similarly, excellent to fair classification (AUROC > 0.75) was observed for ≤2 Gy vs. 7 Gy mice for both genotypes, however, model performance declined (AUROC < 0.75) between genotypes after irradiation. Overall, these results suggest immunosuppression should not compromise small molecule multiplex panels used in dose reconstruction for biodosimetry. ©2022 by Radiation Research Society. All rights of reproduction in any form reserved.

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Year:  2022        PMID: 35245386      PMCID: PMC9214627          DOI: 10.1667/RADE-21-00199.1

Source DB:  PubMed          Journal:  Radiat Res        ISSN: 0033-7587            Impact factor:   3.372


  71 in total

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Journal:  Cell Rep       Date:  2019-07-30       Impact factor: 9.423

2.  Global Gene Expression Response in Mouse Models of DNA Repair Deficiency after Gamma Irradiation.

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Journal:  Radiat Res       Date:  2018-01-19       Impact factor: 2.841

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Journal:  Ther Drug Monit       Date:  2005-12       Impact factor: 3.681

4.  l-carnitine preserves cardiac function by activating p38 MAPK/Nrf2 signalling in hearts exposed to irradiation.

Authors:  Zhigang Fan; Yang Han; Yuanpeng Ye; Chao Liu; Hui Cai
Journal:  Eur J Pharmacol       Date:  2017-04-06       Impact factor: 4.432

5.  Feedback control of the protein kinase TAK1 by SAPK2a/p38alpha.

Authors:  Peter C F Cheung; David G Campbell; Angel R Nebreda; Philip Cohen
Journal:  EMBO J       Date:  2003-11-03       Impact factor: 11.598

6.  Screening of Lipids for Early Triage and Dose Estimation after Acute Radiation Exposure in Rat Plasma Based on Targeted Lipidomics Analysis.

Authors:  Cong Xi; Hua Zhao; Xue Lu; Tian-Jing Cai; Shuang Li; Ke-Hui Liu; Mei Tian; Qing-Jie Liu
Journal:  J Proteome Res       Date:  2020-11-17       Impact factor: 4.466

7.  T cell receptor-mediated activation of p38{alpha} by mono-phosphorylation of the activation loop results in altered substrate specificity.

Authors:  Paul R Mittelstadt; Hiroshi Yamaguchi; Ettore Appella; Jonathan D Ashwell
Journal:  J Biol Chem       Date:  2009-03-25       Impact factor: 5.157

8.  Independent human MAP-kinase signal transduction pathways defined by MEK and MKK isoforms.

Authors:  B Dérijard; J Raingeaud; T Barrett; I H Wu; J Han; R J Ulevitch; R J Davis
Journal:  Science       Date:  1995-02-03       Impact factor: 47.728

Review 9.  The multifaceted roles of PARP1 in DNA repair and chromatin remodelling.

Authors:  Arnab Ray Chaudhuri; André Nussenzweig
Journal:  Nat Rev Mol Cell Biol       Date:  2017-07-05       Impact factor: 94.444

10.  Selective inhibition of the p38 alternative activation pathway in infiltrating T cells inhibits pancreatic cancer progression.

Authors:  Muhammad S Alam; Matthias M Gaida; Frank Bergmann; Felix Lasitschka; Thomas Giese; Nathalia A Giese; Thilo Hackert; Ulf Hinz; S Perwez Hussain; Serguei V Kozlov; Jonathan D Ashwell
Journal:  Nat Med       Date:  2015-10-19       Impact factor: 53.440

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