Bacterial delivery of large intact genomic-DNA containing BACs into mammalian cells

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:2981622 14 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Bacterial delivery of large intact genomic-DNA containing BACs into mammalian cells
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Efficient delivery of large intact vectors into mammalian cells remains problematical. Here we evaluate delivery by bacterial invasion of two large BACs of more than 150 kb in size into various cells. First, we determined the effect of several drugs on bacterial delivery of a small plasmid into different cell lines. Most drugs tested resulted in a marginal increase of the overall efficiency of delivery in only some cell lines, except the lysosomotropic drug chloroquine, which was found to increase the efficiency of delivery by 6-fold in B16F10 cells. Bacterial invasion was found to be significantly advantageous compared with lipofection in delivering large intact BACs into mouse cells, resulting in 100% of clones containing intact DNA. Furthermore, evaluation of expression of the human hypoxanthine phosphoribosy ltransferase (HPRT) gene from its genomic locus, which was present in one of the BACs, showed that single copy integrations of the HPRT-containing BAC had occurred in mouse B16F10 cells and that expression of HPRT from each human copy was 0.33 times as much as from each endogenous mouse copy. These data provide new evidence that bacterial delivery is a convenient and efficient method to transfer large intact therapeutic genes into mammalian cells. © 2012 Landes Bioscience.
Έτος δημοσίευσης:
2012
Συγγραφείς:
Cheung, W.
Kotzamanis, G.
Abdulrazzak, H.
Goussard, S.
Kaname, T.
Kotsinas, A.
Gorgoulis, V.G.
Grillot-Courvalin, C.
Huxley, C.
Περιοδικό:
Bioengineered Bugs
Εκδότης:
Landes Bioscience
Τόμος:
3
Αριθμός / τεύχος:
2
Σελίδες:
86-92
Λέξεις-κλειδιά:
bacterial DNA; chloroquine; complementary DNA; genomic DNA; green fluorescent protein; hypoxanthine phosphoribosyltransferase; methylamine, animal cell; article; bacterial cell; cloning; DNA hybridization; drug delivery system; human; internalization; mammal cell; mouse; nonhuman; nucleus accumbens; pH; plasmid; polymerase chain reaction; protein expression, Bacteria (microorganisms); Mammalia
Επίσημο URL (Εκδότης):
DOI:
10.4161/bbug.18621
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.