Journals / Turkish Journal of Veterinary and Animal Sciences / 2011 / Cilt: 35 - Sayı: 1

Alteration of gene expression in microvascular endothelial cells after exposure to foot-and-mouth disease virus 146S antigen

Pages
21–32
Publication Date
2011-01-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results indicated that the FMDV 146S antigen induces the changes of immune-associated genes in RMMVECs, which suggests that MVECs play an important role in modulating how the innate immune system responds to FMD vaccine.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:To investigate the global response of microvascular endothelial cells (MVECs) to foot-and-mouth (FMDV)disease vaccine (FMDV) antigen and to explore the role of MVECs in FMD vaccine immunity, the gene expression alterations of rat myocardium microvascular endothelial cells (RMMVECs) after stimulation with FMD virus (FMDV) 146S antigen were assayed using cDNA microarrays.
📊
Key Findings & Data:We observed that 18 genes and 67 genes in RMMVECs were respectively altered by FMDV 146S antigen at 6 h and 24 h, respectively.
💡
Conclusion & Impact:The results indicated that the FMDV 146S antigen induces the changes of immune-associated genes in RMMVECs, which suggests that MVECs play an important role in modulating how the innate immune system responds to FMD vaccine.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Microvascular endothelial cells · foot-and-mouth disease virus · 146S

Abstract

To investigate the global response of microvascular endothelial cells (MVECs) to foot-and-mouth (FMDV)disease vaccine (FMDV) antigen and to explore the role of MVECs in FMD vaccine immunity, the gene expression alterations of rat myocardium microvascular endothelial cells (RMMVECs) after stimulation with FMD virus (FMDV) 146S antigen were assayed using cDNA microarrays. We observed that 18 genes and 67 genes in RMMVECs were respectively altered by FMDV 146S antigen at 6 h and 24 h, respectively. The former were all up-regulated genes, and the latter included 60 up-regulated genes and 7 down-regulated genes. Among the differentially expressed genes, many were associated to immune response, such as the genes encoding chemokines, interleukins, complement components, and adhesion molecules. In particular, the chemokine genes had the greatest numbers and significant expression ratios. A part of the altered genes with immune function was validated by real-time reverse transcription-PCR. The influence of FMDV 146S antigen on the secretion of monocyte chemoattractant protein-1, interleukin-6 (IL-6), and IL-1 by RMMVECs was confirmed by enzyme-linked immunosorbent assay, and the expression of vascular cell adhesion molecule-1 was identified by immunocytochemistry. The results indicated that the FMDV 146S antigen induces the changes of immune-associated genes in RMMVECs, which suggests that MVECs play an important role in modulating how the innate immune system responds to FMD vaccine.

Özet

To investigate the global response of microvascular endothelial cells (MVECs) to foot-and-mouth (FMDV)disease vaccine (FMDV) antigen and to explore the role of MVECs in FMD vaccine immunity, the gene expression alterations of rat myocardium microvascular endothelial cells (RMMVECs) after stimulation with FMD virus (FMDV) 146S antigen were assayed using cDNA microarrays. We observed that 18 genes and 67 genes in RMMVECs were respectively altered by FMDV 146S antigen at 6 h and 24 h, respectively. The former were all up-regulated genes, and the latter included 60 up-regulated genes and 7 down-regulated genes. Among the differentially expressed genes, many were associated to immune response, such as the genes encoding chemokines, interleukins, complement components, and adhesion molecules. In particular, the chemokine genes had the greatest numbers and significant expression ratios. A part of the altered genes with immune function was validated by real-time reverse transcription-PCR. The influence of FMDV 146S antigen on the secretion of monocyte chemoattractant protein-1, interleukin-6 (IL-6), and IL-1 by RMMVECs was confirmed by enzyme-linked immunosorbent assay, and the expression of vascular cell adhesion molecule-1 was identified by immunocytochemistry. The results indicated that the FMDV 146S antigen induces the changes of immune-associated genes in RMMVECs, which suggests that MVECs play an important role in modulating how the innate immune system responds to FMD vaccine.

🔖

Cite This Article

ZHANG, T., ZHANG, S., TIAN, L., HU, G., SUO, Z., CHEN, W., DUAN, H., MU, X., TENG, K. (2011). Alteration of gene expression in microvascular endothelial cells after exposure to foot-and-mouth disease virus 146S antigen. Turkish Journal of Veterinary and Animal Sciences, Cilt: 35 - Sayı: 1, 21–32. https://ajindex.com/articles/121531

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Doel, T.R., Chong, W.K.T.: Comparative immunogenicity of 146s, 75s, and 12s particles of FMDV. Arch. Virol., 1982; 73: 185-191. 2. Doel, T.R.: FMD vaccines. Virus Res., 2003; 91: 81-99.
  2. Danese, S., Dejana, E., Claudio, F.: Immune regulation by microvascular endothelial cells: Directing innate and adaptive immunity, coagulation, and infl ammation. J. Immunol., 2007; 178: 6017-6022. Santiago-Delpí n, E.A.: Th e endothelium and early immune activation: New perspective and interactions. News Physiol. Sci., 2004; 16: 84-88.
  3. Cook-Mills, J.M., Deem, T.L.: Active participation of endothelial cells in infl ammation. J. Leukoc. Biol., 2005; 77: 487-495.
  4. Biedermann, B.C.: Vascular endothelium: Checkpoint for infl ammation and immunity. News Physiol. Sci., 2001; 16: 84- 88. 7. Gong, T.L., Sun, L.J., Mao, J.D., Ren, J.Q., Lian, C.Y.: Survey on foot and mouth disease. Journal of Inner Mongolia University for Nationalities, 2001; 16: 393-396.
  5. Hiss, D., Scott-Burden, T., Gevers, W.: Disulfi de-bonded heparan sulfate proteoglycans associated with the surfaces of cultured bovine vascular endothelial cells. Eur. J. Biochem., 1987; 162: 89-94. 9. Monaghan, P., Gold, S., Simpson, J., Zhang, Z., Weinreb, P.H., Violette, S.M., Alexandersen, S., Jackson, T.: Th e integrin αvβ6 receptor for foot-and-mouth disease virus is expressed constitutively on the epithelial cells targeted in cattle. Gen. Virol., 2005; 86: 2769-2780.
  6. Capel-Edwards, M.: Foot-and-mouth disease in the brown rat. J. Comp. Pathol., 1970; 80: 543-548.
  7. Wang, C.Y., Ma, J.W., Fu, X.P.: Purifi cation and examination of foot-and-mouth disease virus. Chinese Journal of Veterinary Science and Technology, 2004; 34: 66-69.
  8. Bradford, M.M.: A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye-binding. Anal. Biochem., 1976; 72: 248-254.
  9. Nishida, M., Carley, W.W., Gerritsen, M.E., Ellingsen, O., Kelly, R.A., Smith, T.W.: Isolation and characterization of human and rat cardiac microvascular endothelial cells. Am. J. Physiol., 1993; 264: H639-H652. Guo, Y., Guo, H., Zhang, L., Xie, H., Zhao, X., Wang, F., Li, Z., Wang, Y., Ma, S., Tao, J., Wang, W., Zhou, Y., Yang, W., Cheng, J.: Genomic analysis of anti-hepatitis B virus (HBV. activity by small interfering RNA and lamivudine in stable HBV-producing cells. J. Virol., 2005; 79: 14392-14403.
  10. Van Gelder, R.N., von Zastrow, M.E., Yool, A., Dement, W.C., Barchas, J.D., Eberwine, J.H.: Amplifi ed RNA synthesized from l