Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (51): 8281-8288.doi: 10.3969/j.issn.2095-4344.2015.51.015

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Programmed cell death 4 is a novel molecular marker of alternatively activated macrophages

Tian Jia1, Jiang Xiao-gang2, Li Hai-yan3, Zhong Bo4, Zhang Fu-jun2, Ning Qi-lan2, Han Yan2, Yang Xu-dong2
 
  

  1. 1Micobiology Institute of Shaanxi, Xi’an 710043, Shaanxi Province, China; 2Department of Biochemistry and Molecule Biology, Preclinical College of Xi’an Jiaotong University, Xi’an 710061, Shaanxi Province, China; 3Department of Pharmacology, Preclinical College of Xi’an Jiaotong University, Xi’an 710061, Shaanxi Province, China; 4Department of Pediatrics, Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
  • Received:2015-09-25 Online:2015-12-10 Published:2015-12-10
  • Contact: Yang Xu-dong, M.D., Lecturer, Department of Biochemistry and Molecule Biology, Preclinical College of Xi’an Jiaotong University, Xi’an 710061, Shaanxi Province, China
  • About author:Tian Jia, Master, Assistant researcher, Micobiology Institute of Shaanxi, Xi’an 710043, Shaanxi Province, China
  • Supported by:

    the National Natural Science Foundation of China, No. 81370123

Abstract:

BACKGROUND: The expression of programmed cell death 4 (PDCD4) is negatively correlated with the phenotype of classically activated macrophages, but the association between PDCD4 and alternative activation of macrophages is undefined.
OBJECTIVE: To explore the changes of PDCD4 expression in alternatively activated macrophages and the effects of PDCD4 on alternative activation.
METHODS: Rat macrophage cell line NR8383 was treated with interleukin-4 and dexamethasone alone or their 
combination to induce alternative activation. Molecular markers of alternatively activated macrophages were detected by qPCR to identify the appropriate conditions for inducing alternative activation. The changes of PDCD4 expression in alternatively activated macrophages were detected by qPCR and western blot. NR8383 was transfected with pEGFP- PDCD4 and shPDCD4 respectively, the efficiency of transfection was evaluated by fluorescence inverted microscope, and the levels of PDCD4 were assayed by qPCR. The molecular markers of classical activation and alternative activation were detected in NR8383 with PDCD4 overexpression or knockdown.
RESULTS AND CONCLUSION: (1) Combination of interleukin-4 and dexamethasone induced the alternative activation of NR8383 more efficiently than interleukin-4 or dexamethasone alone, and alternatively activated macrophages were effectively induced by 10 μg/L interleukin-4+50 nmol/L dexamethasone for 24 hours. (2) The expression of PDCD4 increased significantly in alternatively activated macrophages, which is a novel marker of alternatively activated macrophages. (3) The overexpression of PDCD4 upregulated the expression of Arg-1 and CD206 significantly (P < 0.05); the knockdown of PDCD4 down-regulated the expression of CD206 (P < 0.05), but up-regulated the expression of inducible nitric oxide synthase (P < 0.05). In conclusion, PDCD4 upregulation is an important molecular marker of alternatively activated macrophages. 

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