Research Article: Do derived whitecheek shark proteins motivate T cells to fight cancer cells? A case study in using SW۷۴۲ cell line

Publish Year: 1400
نوع سند: مقاله ژورنالی
زبان: English
View: 232

This Paper With 19 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

این Paper در بخشهای موضوعی زیر دسته بندی شده است:

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_JIFRO-21-2_006

تاریخ نمایه سازی: 16 خرداد 1401

Abstract:

Shark cartilage is considered as a natural dietary supplement consisting of anti-angiogenic, immunostimulatory, and anti-inflammatory characteristics. Therefore, this study was designed to inspect the possibility that whitecheek shark (Carcharhinus dussumieri) cartilage proteins motivate expression of NKG۲D, CXCR۳, NKP۴۶, and NKP۴۴ receptors on natural killer cells and their activities against SW۷۴۲ cell line. To this end, cartilaginous areas of whitecheek shark were caught, minced, stored at −۲۰°C and then lyophilized and kept in refrigerator. Peripheral blood samples were collected from healthy people and a number of ۱۰۶ cells were considered for cell viability using trypan blue method. Activation of NK cells was determined using ۱۰۶ cells stimulated following exposure to ۰.۲ and ۳ mg mL-۱ extracted shark cartilage proteins in ۴, ۸, and ۱۸ h incubation. The results showed that cytotoxicity of NK cells increased significantly by elevating the concentration of extracted proteins at incubation period of ۲۴ h (p˂۰.۰۵). The findings demonstrated that NK activity elevated markedly by increasing the concentration and volume of protein suspension and the exposure time (p˂۰.۰۵). Interestingly, the expression of NKG۲D, CXCR۳, NKP۴۴, and NKP۴۶ receptors was not significant in any transcription level by exposing to ۰, ۲۵, and ۷۵ µg mL-۱ in ۴, ۸, and ۱۸ h incubation period (p˃۰.۰۵). Together, extracted shark cartilage protein could motivate the immune system capabilities through using NK cells against cancer tissues but specific receptors on T cells cannot be activated by these bioactive materials.

Authors

F. Arjmand

Department of Marine Science, Faculty of Natural resources and Environment, Science and Research Branch, Islamic Azad University, Tehran, Iran

A. Sheikhi

Department of Immunology, Faculty of Medicine, Dezful University of Medical Sciences, Azadegan, Dezful, Iran

P. Ghavam Mostafavi

Department of Marine Science, Faculty of Natural resources and Environment, Science and Research Branch, Islamic Azad University, Tehran, Iran

E. Ramezani-Fard

Department of Marine Science, Faculty of Natural resources and Environment, Science and Research Branch, Islamic Azad University, Tehran, Iran

Z. Muhammad Hassan

۵- Department of Immunology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود Paper لینک شده اند :