A method for stimulating the differentiation of human pluripotent stem cells (hPSCs) into kidney lineages remains to be developed. Most cells in kidney are derived from an embryonic germ layer known as intermediate mesoderm (IM). Here we show the establishment of an efficient system of homologous recombination in hPSCs by means of bacterial artificial chromosome (BAC)-based vectors and single nucleotide polymorphism (SNP) array-based detection. This system allowed us to generate human induced pluripotent stem cell (hiPSC) lines containing green fluorescence protein (GFP) knocked into OSR1, a specific marker for IM. We have also established a robust induction protocol for IM, which produces up to 90% OSR1+ cells. These human IM cells can differentiate into multiple cell types of IM-derived organs in vitro and in vivo, thereby supplying an unprecedented system to elucidate the mechanisms of IM development and potentially providing a cell source for regenerative therapies of the kidney.
Historically, the genus Nannochloris has been classified using the morphology of cell division, although the mechanics of division remain relatively poorly understood. Nannochloris bacillaris reproduces by binary fission. Microscopic observation with fluorescein isothiocyanate‐phalloidin showed that actin filaments localized near the nucleus and appeared as a ring‐ or beltlike structure in the septum‐forming area in the middle of the cell during cell division. In primitive unicellular Chlorophyta such as N. bacillaris, actin is also thought to play important roles in nuclear migration and cell division. The N. bacillaris actin gene has three exons and two introns defined by two exon–intron junctions with splice site consensus sequences. The two introns are located at codons specifying amino acids 3/4 and 47/48. One of these, intron position 3/4, is conserved in the actin gene of Saccharomyces cerevisiae. The actin gene product was predicted to be 378 amino acids long with an estimated molecular weight of 42 kDa. There is only one copy of the actin gene in the N. bacillaris genome. Nannochloris bacillaris has 14 chromosomes that range in size from 230 kb to 3000 kb, and the total size of the genome was estimated to be 20.3 Mb. The actin gene is on either chromosome XI or XII. In a phylogenetic tree based on the actin gene sequence, N. bacillaris diverged before the divergence of Volvox, Chlamydomonas, and higher plants, and very shortly after the radiation of the Rhodophyta.
Pseudomonas sp. A-01, isolated as a strain with chitosan-degrading activity, produced a 28 kDa chitosanase. Following purification of the chitosanase (Cto1) and determination of its N-terminal amino acid sequence, the corresponding gene (cto1) was cloned by a reverse-genetic technique. The gene encoded a protein, composed of 266 amino acids, including a putative signal sequence (1-28), that showed an amino acid sequence similar to known family-46 chitosanases. Cto1 was successfully overproduced and was secreted by a Brevibacillus choshinensis transformant carrying the cto1 gene on expression plasmid vector pNCMO2. The purified recombinant Cto1 protein was stable at pH 5-8 and showed the best chitosan-hydrolyzing activity at pH 5. Replacement of two acidic amino acid residues, Glu23 and Asp41, which correspond to previously identified active centers in Streptomyces sp. N174 chitosanase, with Gln and Asn respectively caused a defect in the hydrolyzing activity of the enzyme.
In this study, we induced differentiation of CPT II-deficient hiPSCs into mature myocytes in a highly efficient and reproducible manner and recapitulated some aspects of the disease phenotypes of CPT II deficiency in the myocyte disease models. This approach addresses the challenges of modeling the abnormality of FAO in CPT II deficiency using iPSC technology and has the potential to revolutionize translational research in this field.
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