Proteomic profiling of undifferentiated hBM mesenchymal stem cells under high glucose conditions

Mi Ryung Kim, Ae Jin Choi, Chan Wha Kim

Research output: Contribution to journalArticle

Abstract

Bone marrow mesenchymal stem cells (BM-MSCs) have been suggested to participate in the physiologic healing process of tissue injury by being recruited from the bone marrow and home into the injured site through circulation. To investigate the effect of diabetic hyperglycemia on circulating BM MSCs, which would affect their differentiation, two-dimensional electrophoresis (2-DE) was performed to determine the pattern of protein expression in BM MSCs. After exposure to high (25 mM) glucose concentration for 3 days, six proteins were found to be down regulated by less than 50% (ERp29, Triosephosphate, ATP synthase, phosphoprotein enriched in asprocytes 15, putative glycogen phosphorylase and myosin light chain 3) relative to the control. In addition, 2 proteins (LPLUNC1, isoAsp carboxyl methyltransferase) were neo expressed and one (beta-galactoside binding lectin) protein was shown to be up regulated by more than 300% as a result of hyperglycemia. These results may provide a framework for understanding the molecular mechanism and relationship between hyperglycemia and stem cells.

Original languageEnglish
Pages (from-to)1366-1374
Number of pages9
JournalTissue Engineering and Regenerative Medicine
Volume6
Issue number14
Publication statusPublished - 2009 Dec 1

Fingerprint

Stem cells
Mesenchymal Stromal Cells
Hyperglycemia
Proteomics
Glucose
Proteins
Bone Marrow
Galectins
Glycogen Phosphorylase
Myosin Light Chains
Bone
Phosphoproteins
Methyltransferases
Electrophoresis
Adenosinetriphosphate
Carrier Proteins
Stem Cells
Adenosine Triphosphate
Wounds and Injuries
Tissue

Keywords

  • 2-DE
  • Diabetes
  • HBM-MSCs
  • Hyperglycemia
  • Proteome

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Biomedical Engineering

Cite this

Proteomic profiling of undifferentiated hBM mesenchymal stem cells under high glucose conditions. / Kim, Mi Ryung; Choi, Ae Jin; Kim, Chan Wha.

In: Tissue Engineering and Regenerative Medicine, Vol. 6, No. 14, 01.12.2009, p. 1366-1374.

Research output: Contribution to journalArticle

@article{77086279ade24ea2b44b34eb019f8699,
title = "Proteomic profiling of undifferentiated hBM mesenchymal stem cells under high glucose conditions",
abstract = "Bone marrow mesenchymal stem cells (BM-MSCs) have been suggested to participate in the physiologic healing process of tissue injury by being recruited from the bone marrow and home into the injured site through circulation. To investigate the effect of diabetic hyperglycemia on circulating BM MSCs, which would affect their differentiation, two-dimensional electrophoresis (2-DE) was performed to determine the pattern of protein expression in BM MSCs. After exposure to high (25 mM) glucose concentration for 3 days, six proteins were found to be down regulated by less than 50{\%} (ERp29, Triosephosphate, ATP synthase, phosphoprotein enriched in asprocytes 15, putative glycogen phosphorylase and myosin light chain 3) relative to the control. In addition, 2 proteins (LPLUNC1, isoAsp carboxyl methyltransferase) were neo expressed and one (beta-galactoside binding lectin) protein was shown to be up regulated by more than 300{\%} as a result of hyperglycemia. These results may provide a framework for understanding the molecular mechanism and relationship between hyperglycemia and stem cells.",
keywords = "2-DE, Diabetes, HBM-MSCs, Hyperglycemia, Proteome",
author = "Kim, {Mi Ryung} and Choi, {Ae Jin} and Kim, {Chan Wha}",
year = "2009",
month = "12",
day = "1",
language = "English",
volume = "6",
pages = "1366--1374",
journal = "Tissue Engineering and Regenerative Medicine",
issn = "1738-2696",
publisher = "Springer Science + Business Media",
number = "14",

}

TY - JOUR

T1 - Proteomic profiling of undifferentiated hBM mesenchymal stem cells under high glucose conditions

AU - Kim, Mi Ryung

AU - Choi, Ae Jin

AU - Kim, Chan Wha

PY - 2009/12/1

Y1 - 2009/12/1

N2 - Bone marrow mesenchymal stem cells (BM-MSCs) have been suggested to participate in the physiologic healing process of tissue injury by being recruited from the bone marrow and home into the injured site through circulation. To investigate the effect of diabetic hyperglycemia on circulating BM MSCs, which would affect their differentiation, two-dimensional electrophoresis (2-DE) was performed to determine the pattern of protein expression in BM MSCs. After exposure to high (25 mM) glucose concentration for 3 days, six proteins were found to be down regulated by less than 50% (ERp29, Triosephosphate, ATP synthase, phosphoprotein enriched in asprocytes 15, putative glycogen phosphorylase and myosin light chain 3) relative to the control. In addition, 2 proteins (LPLUNC1, isoAsp carboxyl methyltransferase) were neo expressed and one (beta-galactoside binding lectin) protein was shown to be up regulated by more than 300% as a result of hyperglycemia. These results may provide a framework for understanding the molecular mechanism and relationship between hyperglycemia and stem cells.

AB - Bone marrow mesenchymal stem cells (BM-MSCs) have been suggested to participate in the physiologic healing process of tissue injury by being recruited from the bone marrow and home into the injured site through circulation. To investigate the effect of diabetic hyperglycemia on circulating BM MSCs, which would affect their differentiation, two-dimensional electrophoresis (2-DE) was performed to determine the pattern of protein expression in BM MSCs. After exposure to high (25 mM) glucose concentration for 3 days, six proteins were found to be down regulated by less than 50% (ERp29, Triosephosphate, ATP synthase, phosphoprotein enriched in asprocytes 15, putative glycogen phosphorylase and myosin light chain 3) relative to the control. In addition, 2 proteins (LPLUNC1, isoAsp carboxyl methyltransferase) were neo expressed and one (beta-galactoside binding lectin) protein was shown to be up regulated by more than 300% as a result of hyperglycemia. These results may provide a framework for understanding the molecular mechanism and relationship between hyperglycemia and stem cells.

KW - 2-DE

KW - Diabetes

KW - HBM-MSCs

KW - Hyperglycemia

KW - Proteome

UR - http://www.scopus.com/inward/record.url?scp=84884538963&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84884538963&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:84884538963

VL - 6

SP - 1366

EP - 1374

JO - Tissue Engineering and Regenerative Medicine

JF - Tissue Engineering and Regenerative Medicine

SN - 1738-2696

IS - 14

ER -