Hyperactive RAS/PI3-K/MAPK signaling cascade in migration and adhesion of Nf1 haploinsufficient mesenchymal stem/progenitor cells

Yuan Zhou, Yongzheng He, Richa Sharma, Wen Xing, Selina A. Estwick, Xiaohua Wu, Steven D. Rhodes, Mingjiang Xu, Feng Chun Yang

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Neurofibromatosis type 1 (NF1) is an autosomal dominant disease caused by mutations in the NF1 tumor suppressor gene, which affect approximately 1 out of 3000 individuals. Patients with NF1 suffer from a range of malignant and nonmalignant manifestations such as plexiform neurofibromas and skeletal abnormalities. We previously demonstrated that Nf1 haploinsufficiency in mesenchymal stem/progenitor cells (MSPCs) results in impaired osteoblastic differentiation, which may be associated with the skeletal manifestations in NF1 patients. Here we sought to further ascertain the role of Nf1 in modulating the migration and adhesion of MSPCs of the Nf1 haploinsufficient (Nf1<sup>+/−</sup>) mice. Nf1<sup>+/−</sup>MSPCs demonstrated increased nuclear-cytoplasmic ratio, increased migration, and increased actin polymerization as compared to wild-type (WT) MSPCs. Additionally, Nf1<sup>+/−</sup>MSPCs were noted to have significantly enhanced cell adhesion to fibronectin with selective affinity for CH271 with an overexpression of its complimentary receptor, CD49e. Nf1<sup>+/−</sup>MSPCs also showed hyperactivation of phosphoinositide 3-kinase (PI3-K) and mitogen activated protein kinase (MAPK) signaling pathways when compared to WT MSPCs, which were both significantly reduced in the presence of their pharmacologic inhibitors, LY294002 and PD0325901, respectively. Collectively, our study suggests that both PI3-K and MAPK signaling pathways play a significant role in enhanced migration and adhesion of Nf1 haploinsufficient MSPCs.

Original languageEnglish
Article numberA031
Pages (from-to)12345-12359
Number of pages15
JournalInternational Journal of Molecular Sciences
Volume16
Issue number6
DOIs
StatePublished - 2015

Fingerprint

MAP Kinase Kinase 3
1-Phosphatidylinositol 4-Kinase
stem cells
Phosphatidylinositols
Mitogen-Activated Protein Kinases
Stem cells
Mesenchymal Stromal Cells
cascades
adhesion
Adhesion
proteins
Proteins
Neurofibromatosis 1
tumor suppressor genes
Cell adhesion
abnormalities
mutations
Fibronectins
inhibitors
mice

Keywords

  • Mesenchymal stem/progenitor cells
  • Neurofibroma
  • Neurofibromatosis 1
  • Oncogene protein p21 (ras)

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Spectroscopy
  • Inorganic Chemistry
  • Catalysis
  • Molecular Biology
  • Computer Science Applications

Cite this

Hyperactive RAS/PI3-K/MAPK signaling cascade in migration and adhesion of Nf1 haploinsufficient mesenchymal stem/progenitor cells. / Zhou, Yuan; He, Yongzheng; Sharma, Richa; Xing, Wen; Estwick, Selina A.; Wu, Xiaohua; Rhodes, Steven D.; Xu, Mingjiang; Yang, Feng Chun.

In: International Journal of Molecular Sciences, Vol. 16, No. 6, A031, 2015, p. 12345-12359.

Research output: Contribution to journalArticle

Zhou, Yuan ; He, Yongzheng ; Sharma, Richa ; Xing, Wen ; Estwick, Selina A. ; Wu, Xiaohua ; Rhodes, Steven D. ; Xu, Mingjiang ; Yang, Feng Chun. / Hyperactive RAS/PI3-K/MAPK signaling cascade in migration and adhesion of Nf1 haploinsufficient mesenchymal stem/progenitor cells. In: International Journal of Molecular Sciences. 2015 ; Vol. 16, No. 6. pp. 12345-12359.
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AU - Zhou, Yuan

AU - He, Yongzheng

AU - Sharma, Richa

AU - Xing, Wen

AU - Estwick, Selina A.

AU - Wu, Xiaohua

AU - Rhodes, Steven D.

AU - Xu, Mingjiang

AU - Yang, Feng Chun

PY - 2015

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AB - Neurofibromatosis type 1 (NF1) is an autosomal dominant disease caused by mutations in the NF1 tumor suppressor gene, which affect approximately 1 out of 3000 individuals. Patients with NF1 suffer from a range of malignant and nonmalignant manifestations such as plexiform neurofibromas and skeletal abnormalities. We previously demonstrated that Nf1 haploinsufficiency in mesenchymal stem/progenitor cells (MSPCs) results in impaired osteoblastic differentiation, which may be associated with the skeletal manifestations in NF1 patients. Here we sought to further ascertain the role of Nf1 in modulating the migration and adhesion of MSPCs of the Nf1 haploinsufficient (Nf1+/−) mice. Nf1+/−MSPCs demonstrated increased nuclear-cytoplasmic ratio, increased migration, and increased actin polymerization as compared to wild-type (WT) MSPCs. Additionally, Nf1+/−MSPCs were noted to have significantly enhanced cell adhesion to fibronectin with selective affinity for CH271 with an overexpression of its complimentary receptor, CD49e. Nf1+/−MSPCs also showed hyperactivation of phosphoinositide 3-kinase (PI3-K) and mitogen activated protein kinase (MAPK) signaling pathways when compared to WT MSPCs, which were both significantly reduced in the presence of their pharmacologic inhibitors, LY294002 and PD0325901, respectively. Collectively, our study suggests that both PI3-K and MAPK signaling pathways play a significant role in enhanced migration and adhesion of Nf1 haploinsufficient MSPCs.

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KW - Oncogene protein p21 (ras)

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