Kusworini Handono
Benny Arie Pradana
Radhitio Adi Nugroho
Dian Hasanah
Handono Kalim
Agustina Tri Endharti
Fatchiyah

Abstract

Introduction:

Systemic Lupus Erythematosus (SLE) is a very complicated autoimmune disease which is characterized by the presence of abnormal neutrophils known as Low Density Granulocytes (LDGs). These LDGs have increased capacity to produce Neutrophil Extracellular Traps (NETs). Vitamin D levels in SLE patients were significantly lower than that of healthy subjects. This study aims to investigate the effects of vitamin D [1,25 (OH)2D3] on NETosis and endothelial cell apoptosis in SLE patients with vitamin D deficiency.

Materials and Methods:

Neutrophils of five SLE patients with vitamin D deficiency were treated with four different doses of 1,25 (OH)2D3:0 M as a control, 1x10–9 M, 1x10–8 M, and 10–7M. Phorbol myristate Acetate (PMA) were given to induce production of NETs. The supernatant obtained from NETs induction was cocultured with Human Umbilical Vein Endothelial Cells (HUVECs). Histone and defensin externalization was investigated by immunofluorescence staining. Endothelial apoptosis was investigated by flow cytometry.

Results:

This study shows that neutrophils treated with 1x10–8 M of 1,25 (OH)2D3 had significantly lower defensin, histone externalization, and endothelial cell apoptosis compared to those caused by other doses. There was also a positive correlation between histone externalization and endothelial apoptosis.

Conclusion:

Vitamin D inhibits endothelial damage by reducing the NETs development.

Keywords:

Defensin, endothelial, histone, NETs, 1,25 (OH)2D3, Neutrophil extracellular trap

VOLUME

5

,

ISSUE

3
December 2017

Correspondence

Kusworini Handono

Email

Received

Accepted

Published

Suggested Citation

DOI

License

This work is licensed under the Creative Commons Attribution-NonCommercial-Non-Derivatives 4.0 International License (CC BY-NC-ND 4.0). License