Periostin is temporally expressed as an extracellular matrix component in skeletal muscle regeneration and differentiation

Özdemir, Cansu; Akpulat, Uğur; Sharafi, Parisa; Yıldız, Yılmaz; Onbaşılar, İlyas; Kocaefe, Çetin

doi:10.1016/j.gene.2014.10.014

Cited by 42 publications

(44 citation statements)

References 28 publications

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“…The ECM protein periostin, which exhibited the most significant differential expression in our microarray analysis, is expressed in a variety of tissues during development, including DRG and Schwann cell precursors, as shown by us and others (Kruzynska-Frejtag et al, 2001;Lindsley et al, 2005). So far, several isoforms of periostin with varying domain compositions in the C-terminus, generated through alternative splicing, have been reported (Horiuchi et al, 1999;Litvin et al, 2004;Ozdemir et al, 2014). Using RNA that was isolated from DRG cultures, we could identify five different isoforms, including an isoform that has not been described previously.…”

Section: Discussionsupporting

confidence: 68%

Promotion of periostin expression contributes to the migration of Schwann cells

Sonnenberg-Riethmacher

Miehe

Riethmacher

2015

Journal of Cell Science

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Neuregulin ligands and their ErbB receptors are important for the development of Schwann cells, the glial cells of the peripheral nervous system (PNS). ErbB3 deficiency is characterized by a complete loss of Schwann cells along axons of the peripheral nerves, impaired fasciculation and neuronal cell death. We performed comparative gene expression analysis of dorsal root ganglia (DRG) explant cultures from ErbB3-deficient and wild-type mice in order to identify genes that are involved in Schwann cell development and migration. The extracellular matrix (ECM) gene periostin was found to exhibit the most prominent down regulation in ErbB3-deficient DRG. Expression analysis revealed that the periostin-expressing cell population in the PNS corresponds to Schwann cell precursors and Schwann cells, and is particularly high in migratory Schwann cells. Furthermore, stimulation of Schwann cells with neuregulin-1 (NRG1) or transforming growth factor β (TGFβ-1) resulted in an upregulation of periostin expression. Interestingly, DRG explant cultures of periostindeficient mice revealed a significant reduction of the number of migrating Schwann cells. These data demonstrate that the expression of periostin is stimulated by ErbB ligand NRG1 and influences the migration of Schwann cell precursors.

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Section: Discussionsupporting

confidence: 68%

Promotion of periostin expression contributes to the migration of Schwann cells

Sonnenberg-Riethmacher

Miehe

Riethmacher

2015

Journal of Cell Science

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“…As it was described in several animal studies, periostin is expressed in bones and muscles in response to mechanical stimuli and during post‐exercise regeneration . It may, therefore, be hypothesized that increase in serum periostin in swimmers is because of its constantly repeated release occurring between training sessions.…”

Section: Discussionmentioning

confidence: 86%

Serum but not exhaled breath condensate periostin level is increased in competitive athletes

Kurowski

Jurczyk

Jarzębska

et al. 2018

Clinical Respiratory J

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“…LDB3 plays an important role in the development and maintenance of myofibrils. 41 Fascin homologue 1 (FSCN1) has roles in cell adhesion, motility, and embryogenesis, 42 and it is involved in skeletal muscle development and affecting meat production. 40 POSTN that can alter transforming growth factor β signaling enhances tissue regeneration and dramatically decreases fibrosis.…”

Section: Discussionmentioning

confidence: 99%

A comparison of prenatal muscle transcriptome and proteome profiles between pigs with divergent growth phenotypes

Shang

Wang

Chamba

et al. 2018

J of Cellular Biochemistry

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The growth of pigs is an important economic trait that involves multiple genes and coordinated regulatory mechanisms. The growth rate and potential of skeletal muscles are largely decided by embryonic myofiber development. Tibetan pig (TP) that is a mini‐type breed has a divergent phenotype in growth rate and adult body weight with Wujin pig (WJ) and large White pig (LW). In the current study, the transcriptome (using RNA‐seq) and proteome (using the isobaric tag for relative and absolute quantification [iTRAQ]) data from the prenatal muscle tissues were analyzed to identify the genes related to postnatal growth rate and growth potential in pigs. In the RNA‐seq experiment, 19 626 genes were detected in the embryonic muscle tissues, and 3626 unique differentially expressed genes (DEGs) were identified in TP in comparison to that in LW and WJ. In the iTRAQ experiment, 2474 proteins were detected, and 735 unique differentially expressed proteins (DEPs) were identified in TP in comparison to that in LW and WJ. Combining the DEGs and DEPs, 209 genes were found to be differentially expressed, consistently at both the messenger RNA and protein levels, between TP and the other two breeds; these are mainly involved in 2‐oxocarboxylic acid metabolism, citrate cycle, and biosynthesis of amino acids. Of these, 20 genes that were related to myoblast differentiation and muscle fiber formation might have important roles in determining the postnatal growth rate and potential body weight in pigs. Our results provide new candidate genes and insights into the molecular mechanisms involved muscle growth traits in pigs.

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Periostin is temporally expressed as an extracellular matrix component in skeletal muscle regeneration and differentiation

Cited by 42 publications

References 28 publications

Promotion of periostin expression contributes to the migration of Schwann cells

Promotion of periostin expression contributes to the migration of Schwann cells

Serum but not exhaled breath condensate periostin level is increased in competitive athletes

A comparison of prenatal muscle transcriptome and proteome profiles between pigs with divergent growth phenotypes

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