AI Article Synopsis

  • Subconfluent normal human keratinocytes can grow independently and express specific markers (K5 and K14) related to their proliferation.
  • Researchers used siRNA to knock down PKD1 and found that this led to changes promoting keratinocyte differentiation, evidenced by increased levels of differentiation markers involucrin and K10, while K14 levels remained stable and PCNA levels decreased significantly.
  • The study revealed that PKD1 mRNA is much lower in subconfluent keratinocytes compared to hTert keratinocytes, indicating a potentially different role of PKD1 in primary versus immortalized keratinocyte cultures.

Article Abstract

Subconfluent normal human keratinocytes exhibit autonomous (autocrine growth factor driven) proliferation and express the specific markers for keratinocyte proliferation K5 (keratin 5) and K14 (keratin 14). Utilizing this model the effects of PKD1 (Protein kinase D1) knockdown on activation of differentiation was studied. siRNA approach was applied to achieve specific knockdown of PKD1 and the mRNA levels of different keratinocyte markers -- K14 and PCNA (markers of basal proliferating keratinocytes), involucrin and K10 (early differentiation markers) were analyzed. Treatment of cultured keratinocytes with siRNA for PKD1 resulted in reduction of mRNA levels of PKD1, altered cell phenotype and promotion of keratinocyte differentiation, demonstrated by increased expression of involucrin and K10 mRNAs. No significant changes in K14 mRNA expression levels were detected, but the expression of PCNA mRNA was markedly diminished. This study was the first to show that mRNA expression of PKD1 in subconfluent normal human keratinocytes is very low, the PKD1 mRNA levels were more than 8-fold lower than the same ones in hTert keratinocytes. These findings suggest antidifferentiative role of PKD1 in normal human keratinocytes, contrary to the prodiferentiative role of PKD1 in human hTert keratinocytes. We came to the conclusion that there are differences between transduction pathways involving PKD1 in primary human keratinocyte cultures and these in immortalized hTert keratinocytes.

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http://dx.doi.org/10.1007/s00403-008-0832-7DOI Listing

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