CXC chemokine receptor 4 is essential for Lipo-PGE1-enhanced migration of human dermal fibroblasts

Yoolhee Yang, Su Kyung Shim, Hyun A. Kim, Mira Seon, Eunjung Yang, Dae Ho Cho, Sa Ik Bang

Research output: Contribution to journalLetter

9 Citations (Scopus)

Abstract

Lipo-PGE1 [EGLANDIN ®; a lipid microsphere-incorporated prostaglandin E1 (PGE1)] stimulates angiogenesis and promotes the healing of skin ulcers. Because the effects of Lipo-PGE1 on cutaneous wound healing are not completely understood, we investigated the ability of Lipo-PGE1 to affect in vivo wound healing and regulate the migration of human dermal fibroblasts (HDFs). In a murine wound model, Lipo-PGE1 reduced the wound size compared with control mice. Lipo-PGE1 significantly increased HDF migration in a dose- and time-dependent manner. Lipo-PGE1 markedly increased the expression of CXC chemokine receptor 4 (CXCR4), which controls the migration of HDFs, at the mRNA and protein levels. Small interfering RNA (siRNA)-mediated knockdown of CXCR4 inhibited Lipo-PGE1-enhanced HDF migration. Moreover, Lipo-PGE1 directly induced the phosphorylation of c-Jun N-terminal kinase (JNK), and the JNK-specific inhibitor Sp6000125 blocked Lipo-PGE1-enhanced migration and CXCR4 expression of HDFs. Our results demonstrate that Lipo-PGE1 accelerates wound healing in vivo and increases the CXCR4-mediated migration of HDFs through the JNK pathway.

Original languageEnglish
Pages (from-to)75-77
Number of pages3
JournalExperimental Dermatology
Volume21
Issue number1
DOIs
Publication statusPublished - 2012 Jan 1
Externally publishedYes

Fingerprint

CXCR4 Receptors
Alprostadil
Fibroblasts
Skin
Wound Healing
Phosphotransferases
Skin Ulcer
Phosphorylation
JNK Mitogen-Activated Protein Kinases
Wounds and Injuries
Microspheres
Small Interfering RNA

Keywords

  • CXC chemokine receptor 4
  • Human dermal fibroblasts (HDFs)
  • Lipo-PGE1
  • Migration
  • Wound healing

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Dermatology

Cite this

CXC chemokine receptor 4 is essential for Lipo-PGE1-enhanced migration of human dermal fibroblasts. / Yang, Yoolhee; Shim, Su Kyung; Kim, Hyun A.; Seon, Mira; Yang, Eunjung; Cho, Dae Ho; Bang, Sa Ik.

In: Experimental Dermatology, Vol. 21, No. 1, 01.01.2012, p. 75-77.

Research output: Contribution to journalLetter

Yang, Yoolhee ; Shim, Su Kyung ; Kim, Hyun A. ; Seon, Mira ; Yang, Eunjung ; Cho, Dae Ho ; Bang, Sa Ik. / CXC chemokine receptor 4 is essential for Lipo-PGE1-enhanced migration of human dermal fibroblasts. In: Experimental Dermatology. 2012 ; Vol. 21, No. 1. pp. 75-77.
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abstract = "Lipo-PGE1 [EGLANDIN {\circledR}; a lipid microsphere-incorporated prostaglandin E1 (PGE1)] stimulates angiogenesis and promotes the healing of skin ulcers. Because the effects of Lipo-PGE1 on cutaneous wound healing are not completely understood, we investigated the ability of Lipo-PGE1 to affect in vivo wound healing and regulate the migration of human dermal fibroblasts (HDFs). In a murine wound model, Lipo-PGE1 reduced the wound size compared with control mice. Lipo-PGE1 significantly increased HDF migration in a dose- and time-dependent manner. Lipo-PGE1 markedly increased the expression of CXC chemokine receptor 4 (CXCR4), which controls the migration of HDFs, at the mRNA and protein levels. Small interfering RNA (siRNA)-mediated knockdown of CXCR4 inhibited Lipo-PGE1-enhanced HDF migration. Moreover, Lipo-PGE1 directly induced the phosphorylation of c-Jun N-terminal kinase (JNK), and the JNK-specific inhibitor Sp6000125 blocked Lipo-PGE1-enhanced migration and CXCR4 expression of HDFs. Our results demonstrate that Lipo-PGE1 accelerates wound healing in vivo and increases the CXCR4-mediated migration of HDFs through the JNK pathway.",
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