AI Article Synopsis

  • Keratinocytes are challenging to genetically modify, and viral vectors are effective alternatives for this purpose.
  • A traditional method involves using retroviral vectors and co-culturing keratinocytes with virus-producing cells, which is efficient in high-calcium environments but can be labor-intensive.
  • This chapter offers enhanced protocols for stable genetic modification of human primary keratinocytes using lentiviral vectors, suitable for both low- and high-calcium conditions.

Article Abstract

Keratinocytes are hard to transfect. Viral vectors are a good alternative to genetically modify primary keratinocytes. A classical method is the use of retroviral vectors by co-culture of keratinocytes with virus-producer cells. This method is efficient in high-calcium conditions with feeder cells. However, sometimes co-culture is not possible and is more laborious as producer cells need to be replaced by feeder cells. Our solution is the use of lentiviral vectors, far more efficient as supernatant on keratinocytes. In this chapter we describe improved detailed protocols for stable genetic modification of human primary keratinocytes of the skin or head and neck, in both low- and high-calcium conditions by lentiviral vectors.

Download full-text PDF

Source
http://dx.doi.org/10.1007/7651_2019_238DOI Listing

Publication Analysis

Top Keywords

primary keratinocytes
12
lentiviral vectors
12
genetic modification
8
modification human
8
human primary
8
high-calcium conditions
8
feeder cells
8
keratinocytes
6
vectors
5
keratinocytes lentiviral
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!