Protein Kinase C and Toll-Like Receptor Signaling

المؤلفون المشاركون

Lennartz, Michelle R.
Loegering, Daniel J.

المصدر

Enzyme Research

العدد

المجلد 2011، العدد 2011 (31 ديسمبر/كانون الأول 2011)، ص ص. 1-7، 7ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2011-08-23

دولة النشر

مصر

عدد الصفحات

7

التخصصات الرئيسية

الأحياء

الملخص EN

Protein kinase C (PKC) is a family of kinases that are implicated in a plethora of diseases, including cancer and cardiovascular disease.

PKC isoforms can have different, and sometimes opposing, effects in these disease states.

Toll-like receptors (TLRs) are a family of pattern recognition receptors that bind pathogens and stimulate the secretion of cytokines.

It has long been known that PKC inhibitors reduce LPS-stimulated cytokine secretion by macrophages, linking PKC activation to TLR signaling.

Recent studies have shown that PKC-α, -δ, -ε, and -ζ are directly involved in multiple steps in TLR pathways.

They associate with the TLR or proximal components of the receptor complex.

These isoforms are also involved in the downstream activation of MAPK, RhoA, TAK1, and NF-κB.

Thus, PKC activation is intimately involved in TLR signaling and the innate immune response.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Loegering, Daniel J.& Lennartz, Michelle R.. 2011. Protein Kinase C and Toll-Like Receptor Signaling. Enzyme Research،Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-479652

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Loegering, Daniel J.& Lennartz, Michelle R.. Protein Kinase C and Toll-Like Receptor Signaling. Enzyme Research No. 2011 (2011), pp.1-7.
https://search.emarefa.net/detail/BIM-479652

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Loegering, Daniel J.& Lennartz, Michelle R.. Protein Kinase C and Toll-Like Receptor Signaling. Enzyme Research. 2011. Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-479652

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-479652