Literature DB >> 15313414

High mobility group box 1 protein, a cue for stem cell recruitment.

Roberta Palumbo1, Marco E Bianchi.   

Abstract

High mobility group box 1 (HMGB1) is a non-histone protein required to maintain chromatin architecture. Recent observations demonstrated that HMGB1 can also act as a cytokine to regulate different biological processes such as inflammation, cell migration and metastasis. We showed previously that HMGB1 can be released passively by cells that die in a traumatic and unprogrammed way, and can serve a signal of tissue damage. More recently, we showed that HMGB1 can recruit stem cells: HMGB1 induces stem cell transmigration through an endothelial barrier; moreover, when beads containing HMGB1 are implanted into healthy muscle, they recruit stem cells injected into the general circulation. The inflammatory and tissue-regenerating roles of HMGB1 may be strictly interconnected, and are discussed here.

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Year:  2004        PMID: 15313414     DOI: 10.1016/j.bcp.2004.03.048

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  36 in total

1.  Toll-like receptor deficiency worsens inflammation and lymphedema after lymphatic injury.

Authors:  Jamie C Zampell; Sonia Elhadad; Tomer Avraham; Evan Weitman; Seth Aschen; Alan Yan; Babak J Mehrara
Journal:  Am J Physiol Cell Physiol       Date:  2011-11-02       Impact factor: 4.249

2.  Damage-associated molecular patterns (DAMPs) in preterm labor with intact membranes and preterm PROM: a study of the alarmin HMGB1.

Authors:  Roberto Romero; Tinnakorn Chaiworapongsa; Zeynep Alpay Savasan; Yi Xu; Youssef Hussein; Zhong Dong; Juan Pedro Kusanovic; Chong Jai Kim; Sonia S Hassan
Journal:  J Matern Fetal Neonatal Med       Date:  2011-09-29

Review 3.  Brain-peripheral cell crosstalk in white matter damage and repair.

Authors:  Kazuhide Hayakawa; Eng H Lo
Journal:  Biochim Biophys Acta       Date:  2015-08-13

4.  The IKKα-dependent NF-κB p52/RelB noncanonical pathway is essential to sustain a CXCL12 autocrine loop in cells migrating in response to HMGB1.

Authors:  Richard R Kew; Marianna Penzo; David M Habiel; Kenneth B Marcu
Journal:  J Immunol       Date:  2012-01-27       Impact factor: 5.422

5.  Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy.

Authors:  Cristina Sancricca; Massimiliano Mirabella; Carla Gliubizzi; Aldobrando Broccolini; Teresa Gidaro; Roberta Morosetti
Journal:  World J Stem Cells       Date:  2010-06-26       Impact factor: 5.326

Review 6.  In situ tissue regeneration: chemoattractants for endogenous stem cell recruitment.

Authors:  Wendy S Vanden Berg-Foels
Journal:  Tissue Eng Part B Rev       Date:  2013-07-11       Impact factor: 6.389

Review 7.  A review of metabolic staging in severely injured patients.

Authors:  Maria-Angeles Aller; Jose-Ignacio Arias; Alfredo Alonso-Poza; Jaime Arias
Journal:  Scand J Trauma Resusc Emerg Med       Date:  2010-05-17       Impact factor: 2.953

Review 8.  The HMGB1-RAGE Inflammatory Pathway: Implications for Brain Injury-Induced Pulmonary Dysfunction.

Authors:  Daniel J Weber; Yohance M Allette; David S Wilkes; Fletcher A White
Journal:  Antioxid Redox Signal       Date:  2015-05-14       Impact factor: 8.401

9.  Amino acid residues 201-205 in C-terminal acidic tail region plays a crucial role in antibacterial activity of HMGB1.

Authors:  Wei Gong; Yuan Li; Fan Chao; Gang Huang; Fengtian He
Journal:  J Biomed Sci       Date:  2009-09-14       Impact factor: 8.410

10.  Haematopoietic stem cell migration to the ischemic damaged kidney is not altered by manipulating the SDF-1/CXCR4-axis.

Authors:  Ingrid Stroo; Geurt Stokman; Gwendoline J D Teske; Sandrine Florquin; Jaklien C Leemans
Journal:  Nephrol Dial Transplant       Date:  2009-02-16       Impact factor: 5.992

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