Expression of c-kit receptor in peripheral blood mononuclear cells in patients with systemic lupus erythematosus
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Maihua Hou Lingyun Sun and Xinzheng Lu Department of Dermatology the First Affiliated Hospital of Nanjing Medical University Nanjing
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Maihua Hou Lingyun Sun and Xinzheng Lu Department of Dermatology the First Affiliated Hospital of Nanjing Medical University Nanjing
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Department of Rheumatology and Immunology Nanjing Drum Tower Hospital Nanjing University Medical School Nanjing
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Department of Rheumatology and Immunology Nanjing Drum Tower Hospital Nanjing University Medical School Nanjing
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Department of Cardiology the First Affiliated Hospital of Nanjing Medical University Nanjing China
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Department of Cardiology the First Affiliated Hospital of Nanjing Medical University Nanjing China
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Objective: To determine the expression of c-kit receptor in peripheral blood mononuclear cells (PBMCs) in patients with systemic lupus erythematosus (SLE), and analyze the relationship between the c-kit expression level of PBMCs and clinical parameters. Methods: Peripheral blood mononuclear cells in 47 patients with SLE and 21 healthy volunteers were collected. Expression of c-kit mRNA in PBMCs were determined with reverse transcription-polymerase chain reaction (RT-PCR). The protein of c-kit receptor (CD117) in PBMCs was measured by flow cytometry. Results: Expression of c-kit receptor protein and mRNA in patients with active or inactive SLE (n=47) were significantly higher than those in controls. The c-kit receptor of PBMCs in SLE patients were significantly higher than those in healthy controls (n=21), the c-kit receptor of PBMCs in active patients (n=27) were significantly higher than those in inactive patients (n=20) and there was no significant difference was found between patients with inactive SLE and healthy controls(P>0.05). The c-kit receptor of PBMCs in SLE have significant association with activity index. Conclusion: Production of c-kit receptor is aberrantly increased in PBMCs in patients with SLE. C-kit receptor might be more closely related to the clinical parameters in SLE patients, which might reflect the clinical status of SLE patients.
Mutaltions of c-kit JM domain are found in amino rity of human gastrointestinal stromal tu- mors .2 Moskaluk CA,Tian Q,Marshall CR,et al. Oncogene . 1999
Mutaltions of c-kit JM domain are found in amino rity of human gastrointestinal stromal tu- mors .2 Moskaluk CA,Tian Q,Marshall CR,et al. Oncogene . 1999