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1.
Ecol Evol ; 3(10): 3447-54, 2013 Sep.
Article in English | MEDLINE | ID: mdl-24223281

ABSTRACT

Wheat (Triticum aestivum L.) is one of the most successful domesticated plant species in the world. The majority of wheat carries mutations in the Puroindoline genes that result in a hard kernel phenotype. An evolutionary explanation, or selective advantage, for the spread and persistence of these hard kernel mutations has yet to be established. Here, we demonstrate that the house mouse (Mus musculus L.) exerts a pronounced feeding preference for soft over hard kernels. When allele frequencies ranged from 0.5 to 0.009, mouse predation increased the hard allele frequency as much as 10-fold. Studies involving a single hard kernel mixed with ∼1000 soft kernels failed to recover the mutant kernel. Nevertheless, the study clearly demonstrates that the house mouse could have played a role in the evolution of wheat, and therefore the cultural trajectory of humankind.

2.
Theor Appl Genet ; 124(6): 1079-96, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22186959

ABSTRACT

Wheat is marketed based on end-use quality characteristics and better knowledge of the underlying genetics of specific quality parameters is essential to enhance the breeding process. A set of 188 recombinant inbred lines from a 'Louise' by 'Penawawa' mapping population was grown in two crop years at two locations in the Pacific Northwest region of the United States and data were collected on 17 end-use quality traits using established quality analysis protocols. Using an established genetic linkage map, composite interval mapping was used to identify QTL associated with 16 of the 17 quality traits. QTL were found on 13 of the 21 wheat chromosomes. A large number of QTL were located on chromosomes 3B and 4D and coincided with traits for milling quality and starch functionality. Chromosome 3B contained 10 QTL, which were localized to a 26.2 cM region. Chromosome 4D contained 7 QTL, all of which were located on an 18.8 cM region of this chromosome. The majority of the alleles for superior end-use quality were associated with the cultivar Louise. The identified QTL detected remained highly significant independent of grain yield and protein quantity. The identification of these QTL for end-use quality gives key insight into the relationship and complexity of end-use quality traits. It also improves our understanding of these relationships, thereby allowing plant breeders to make valuable gains from selection for these important traits.


Subject(s)
Chromosomes, Plant/genetics , Quantitative Trait Loci , Triticum/genetics , Alleles , Breeding , Chromosome Mapping/methods , Crosses, Genetic , DNA, Plant/genetics , Genes, Plant , Genetic Linkage , Northwestern United States , Phenotype , Seasons , Sequence Analysis, DNA
3.
Food Sci Technol Int ; 16(6): 511-22, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21339167

ABSTRACT

Wheat quality, a complex term, depends upon intentional use for unambiguous products. The foremost determinants of wheat quality are endosperm texture (grain hardness), protein content and gluten strength. Endosperm texture in wheat is the single most important and defining quality characteristic, as it facilitates wheat classification and affects milling, baking and end-use quality. Various techniques used for grain hardness measurement are classified into diverse groups according to grinding, crushing and abrasion. The most extensively used methods for texture measurement are PSI, NIR hardness, SKCS, pearling index, SDS-PAGE and PCR markers. Friabilin is a 15 kDa endosperm specific protein associated with starch granules of wheat grain and is unswervingly related to grain softness. Chemically, it is a concoction of different polypeptides, primarily puroindolines; Pin a and Pin b. Hardness (Ha) locus of chromosome 5DS makes the distinction between soft and hard classes of wheat. Some additional modifying genes are also present which contribute to the disparity within wheat classes. Numerous allelic mutations in Pin have been reported and their relation to end product quality has been established. This treatise elaborates the consequence of grain hardness in wheat eminence.


Subject(s)
Seeds/chemistry , Triticum/chemistry , Triticum/classification , Chemical Phenomena , Edible Grain , Endosperm/chemistry , Flour/analysis , Glutens/analysis , Glutens/chemistry , Mechanical Phenomena , Plant Proteins/analysis , Plant Proteins/chemistry , Triticum/genetics
4.
Protein Pept Lett ; 15(9): 995-1001, 2008.
Article in English | MEDLINE | ID: mdl-18991777

ABSTRACT

The present review brings a timeline of some of the major steps given throughout the years towards the development of our knowledge regarding the biology of the neutrophil. The contribution of early articles and their elementary biochemical approach is highlighted. The importance of the development of proteomic techniques is paralleled to the shift in neutrophil research towards high throughput molecular methods. As a last change of standpoint, the study of the neutrophil is presented integrated with other life- sciences technologies such as lipidomics, genomics and systems biology. The paper also brings a perspective/tendency overview at the same time that it discusses some of the difficulties encountered in the research of the neutrophil.


Subject(s)
Neutrophils/chemistry , Neutrophils/metabolism , Proteome , Proteomics/methods , Chromatography, High Pressure Liquid , Electrophoresis, Gel, Two-Dimensional , Humans , Neutrophils/physiology , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Tandem Mass Spectrometry
5.
Theor Appl Genet ; 115(1): 47-58, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17426955

ABSTRACT

Polyphenol oxidase (PPO) activity is highly related to the undesirable browning of wheat-based end products, especially Asian noodles. Characterization of PPO genes and the development of their functional markers are of great importance for marker-assisted selection in wheat breeding. In the present study, complete genomic DNA sequences of two PPO genes, one each located on chromosomes 2A and 2D and their allelic variants were characterized by means of in silico cloning and experimental validation. Sequences were aligned at both DNA and protein levels. Two haplotypes on chromosome 2D showed 95.2% sequence identity at the DNA level, indicating much more sequence diversity than those on chromosome 2A with 99.6% sequence identity. Both of the PPO genes on chromosomes 2A and 2D contain an open reading frame (ORF) of 1,731 bp, encoding a PPO precursor peptide of 577 amino acids with a predicted molecular mass of approximately 64 kD. Two complementary dominant STS markers, PPO16 and PPO29, were developed based on the PPO gene haplotypes located on chromosome 2D; they amplify a 713-bp fragment in cultivars with low PPO activity and a 490-bp fragment in those with high PPO activity, respectively. The two markers were mapped on chromosome 2DL using a doubled haploid population derived from the cross Zhongyou 9507/CA9632, and a set of nullisomic-tetrasomic lines and ditelosomic line 2DS of Chinese Spring. QTL analysis indicated that the PPO gene co-segregated with the two STS markers and was closely linked to SSR marker Xwmc41 on chromosome 2DL, explaining from 9.6 to 24.4% of the phenotypic variance for PPO activity across three environments. In order to simultaneously detect PPO loci on chromosomes 2A and 2D, a multiplexed marker combination PPO33/PPO16 was developed and yielded distinguishable DNA patterns in a number of cultivars. The STS marker PPO33 for the PPO gene on chromosome 2A was developed from the same gene sequences as PPO18 that we reported previously, and can amplify a 481-bp and a 290-bp fragment from cultivars with low and high PPO activity, respectively. A total of 217 Chinese wheat cultivars and advanced lines were used to validate the association between the polymorphic fragments and grain PPO activity. The results showed that the marker combination PPO33/PPO16 is efficient and reliable for evaluating PPO activity and can be used in wheat breeding programs aimed for noodle and other end product quality improvement.


Subject(s)
Alleles , Catechol Oxidase/genetics , Chromosomes, Plant/genetics , Genetic Variation , Triticum/enzymology , Triticum/genetics , Amino Acid Sequence , Base Sequence , Catechol Oxidase/physiology , Genetic Markers/physiology , Molecular Sequence Data , Triticum/physiology
6.
Theor Appl Genet ; 112(3): 400-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16344983

ABSTRACT

Kernel hardness that is conditioned by puroindoline genes has a profound effect on milling, baking and end-use quality of bread wheat. In this study, 219 landraces and 166 historical cultivars from China and 12 introduced wheats were investigated for their kernel hardness and puroindoline alleles, using molecular and biochemical markers. The results indicated that frequencies of soft, mixed and hard genotypes were 42.7, 24.3, and 33.0%, respectively, in Chinese landraces and 45.2, 13.9, and 40.9% in historical cultivars. The frequencies of PINA null, Pinb-D1b and Pinb-D1p genotypes were 43.8, 12.3, and 39.7%, respectively, in hard wheat of landraces, while 48.5, 36.8, and 14.7%, respectively, in historical hard wheats. A new Pinb-D1 allele, designated Pinb-D1t, was identified in two landraces, Guangtouxianmai and Hongmai from the Guizhou province, with the characterization of a glycine to arginine substitution at position 47 in the coding region of Pinb gene. Surprisingly, a new Pina-D1 allele, designated Pina-D1m, was detected in the landrace Hongheshang, from the Jiangsu province, with the characterization of a proline to serine substitution at position 35 in the coding region of Pina gene; it was the first novel mutation found in bread wheat, resulting in a hard endosperm with PINA expression. Among the PINA null genotypes, an allele designed as Pina-D1l, was detected in five landraces with a cytosine deletion at position 265 in Pina locus; while another novel Pina-D1 allele, designed as Pina-D1n, was identified in six landraces, with the characterization of an amino acid change from tryptophan-43 to a 'stop' codon in the coding region of Pina gene. The study of puroindoline polymorphism in Chinese wheat germplasm could provide useful information for the further understanding of the molecular basis of kernel hardness in bread wheat.


Subject(s)
Alleles , Plant Proteins/genetics , Plant Proteins/metabolism , Triticum/genetics , Triticum/metabolism , Amino Acid Sequence , Amino Acid Substitution , Arginine/metabolism , Base Sequence , Biomarkers , China , DNA, Plant/chemistry , DNA, Plant/isolation & purification , Electrophoresis, Polyacrylamide Gel , Gene Deletion , Gene Frequency , Genes, Plant , Genetic Variation , Genotype , Molecular Sequence Data , Plant Proteins/chemistry , Plant Proteins/isolation & purification , Polymorphism, Genetic , Seeds/genetics , Sequence Analysis, DNA , Serine/metabolism , Species Specificity , Triticum/physiology
7.
Theor Appl Genet ; 109(8): 1597-603, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15448897

ABSTRACT

Aegilops tauschii (2 n=2 x=14, DD) is a rich source of genetic variability for hexaploid wheat ( Triticum aestivum, 2 n=6 x=42, AABBDD) improvement. This variability can be accessed through utilizing synthetic hexaploid wheat lines, which contain genomes from Ae. tauschii and T. turgidum (2 n=4 x=28, AABB). Numerous desirable characteristics can and have been introgressed into common hexaploid wheat with this germplasm. In this work, the genetic variability in the two puroindoline genes (a and b) contained on the D genome, and the relationship that sequence polymorphisms in these genes have on endosperm texture among a population of 75 CIMMYT synthetic hexaploid accessions is described. Kernel texture was evaluated using the single kernel characterization system (SKCS). Kernel texture differed significantly ( P

Subject(s)
Crops, Agricultural/genetics , Hybridization, Genetic , Plant Proteins/genetics , Polyploidy , Seeds/anatomy & histology , Triticum/genetics , Agriculture/methods , Amino Acid Sequence , Analysis of Variance , Base Sequence , Gene Transfer Techniques , Molecular Sequence Data , Seeds/chemistry , Sequence Alignment , Sequence Analysis, DNA
8.
Genome ; 45(3): 584-91, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12033628

ABSTRACT

Endosperm texture has a tremendous impact on the end-use quality of wheat (Triticum aestivum L.). Cultivars of barley (Hordeum vulgare L.), a close relative of wheat, also vary measurably in grain hardness. However, in contrast to wheat, little is known about the genetic control of barley grain hardness. Puroindolines are endosperm-specific proteins found in wheat and its relatives. In wheat, puroindoline sequence variation controls the majority of wheat grain texture variation. Hordoindolines, the puroindoline homologs of barley, have been identified and mapped. Recently, substantial allelic variation was found for hordoindolines among commercial barley cultivars. Our objective was to determine the influence of hordoindoline allelic variation upon grain hardness and dry matter digestibility in the 'Steptoe' x 'Morex' mapping population. This population is segregating for hordoindoline allele type, which was measured by a HinA/HinB/Gsp composite marker. One-hundred and fifty lines of the 'Steptoe' x 'Morex' population were grown in a replicated field trial. Grain hardness was estimated by near-infrared reflectance (NIR) and measured using the single kernel characterization system (SKCS). Variation attributable to the HinA/HinB/Gsp locus averaged 5.7 SKCS hardness units (SKCS U). QTL analysis revealed the presence of several areas of the genome associated with grain hardness. The largest QTL mapped to the HinA/HinB/Gsp region on the short arm of chomosome 7 (5H). This QTL explains 22% of the SKCS hardness difference observed in this study. The results indicate that the Hardness locus is present in barley and implicates the hordoindolines in endosperm texture control.


Subject(s)
Hordeum/genetics , Quantitative Trait Loci , Plant Proteins/genetics , Seeds/metabolism
9.
Transplantation ; 67(7): 963-71, 1999 Apr 15.
Article in English | MEDLINE | ID: mdl-10221479

ABSTRACT

BACKGROUND: Previous in vivo depletion studies of CD4 and CD8 T cells indicated that different rejection mechanisms operate for proislet allografts and xenografts. The cellular and molecular mechanisms of acute proislet allograft and xenograft rejection have therefore been characterized and directly compared. METHODS: The intragraft cytokine mRNA profile in rejecting BALB/c (H-2d) proislet allografts was analyzed in control, CD4 T cell-depleted, and CD8 T cell-depleted CBA/H (H-2k) recipient mice using semi-quantitative reverse transcriptase-assisted polymerase chain reaction (RT-PCR). The cytokine profiles for proislet allografts and pig proislet xenografts at 3-10 days posttransplant were directly compared and correlated with graft histopathology. RESULTS: Allograft rejection was protracted (2-3 weeks), characterized by infiltrating CD8 T cells and CD4 T cells (no eosinophils) and was associated with a Th1-type CD4 T cell response (IL-2, IFN-gamma, and IL-3 mRNA) and a CD8 T cell-dependent spectrum of cytokine gene expression (IL-2, IFN-gamma, IL-3, and IL-10 mRNA). Xenograft rejection was rapid (6-8 days), involved predominantly CD4 T cells and eosinophils, and in contrast to allografts, exhibited intragraft mRNA expression for the Th2 cytokines IL-4 and IL-5. CONCLUSIONS: Proislet allograft and xenograft rejection differ in the tempo of destruction, phenotype of the cellular response and intragraft profile of cytokine mRNA. The recruitment of eosinophils only to the site of xenorejection correlates with IL4 and IL-5 mRNA expression. These findings suggest that different anti-rejection strategies may need to be developed to optimally target the allograft and the xenograft response.


Subject(s)
Fetal Tissue Transplantation/immunology , Graft Rejection/immunology , Islets of Langerhans Transplantation/immunology , Islets of Langerhans/embryology , Transplantation, Heterologous/immunology , Animals , Cytokines/genetics , Fetus/anatomy & histology , Fetus/metabolism , Graft Rejection/metabolism , Graft Rejection/pathology , Immunohistochemistry , Islets of Langerhans/metabolism , Islets of Langerhans/pathology , Male , Mice , Mice, Inbred BALB C , Mice, Inbred CBA , RNA, Messenger/metabolism , Swine , Transplantation, Homologous/immunology
10.
Biochemistry ; 38(8): 2523-34, 1999 Feb 23.
Article in English | MEDLINE | ID: mdl-10029547

ABSTRACT

Keratinocyte growth factor (KGF or FGF-7) is a member of the heparin binding fibroblast growth factor (FGF) family and is a paracrine mediator of proliferation and differentiation of a wide variety of epithelial cells. To examine the stoichiometry of complexes formed between KGF and its receptor, we have utilized a soluble variant of the extracellular region of the KGF receptor containing two tandem immunoglobulin-like loops, loops II and III (sKGFR). Ligand-receptor complexes were examined by size exclusion chromatography, light scattering, N-terminal protein sequencing, and sedimentation velocity. In the presence of low-molecular mass heparin ( approximately 3 kDa), we demonstrate the formation of complexes containing two molecules of sKGFR and one molecule of KGF. In the absence of heparin, we were unable to detect any KGF-sKGFR complexes using the above techniques, and additional studies in which sedimentation equilibrium was used show that the binding is very weak (Kd >/= 70 microM). Furthermore, using heparin fragments of defined size, we demonstrate that a heparin octamer or decamer can promote formation of a 2:1 complex, while a hexamer does not. Utilizing the highly purified proteins and defined conditions described in this study, we find that heparin is obligatory for formation of a KGF-sKGFR complex. Finally, 32D cells, which appear to lack low-affinity FGF binding sites, were transfected with a KGFR-erythropoeitin receptor chimera and were found to require heparin to achieve maximal KGF stimulation. Our data are consistent with the previously described concept that cell- or matrix-associated heparan sulfate proteoglycans (HSPGs) and FGF ligands participate in a concerted mechanism that facilitates FGFR dimerization and signal transduction in vivo.


Subject(s)
Extracellular Space/metabolism , Fibroblast Growth Factors , Growth Substances/metabolism , Heparin/physiology , Keratinocytes/metabolism , Peptide Fragments/metabolism , Receptors, Fibroblast Growth Factor , Receptors, Growth Factor/metabolism , Amino Acid Sequence , Cell Division/drug effects , Cell Line , Chromatography, Gel , DNA/biosynthesis , Dimerization , Extracellular Space/chemistry , Fibroblast Growth Factor 10 , Fibroblast Growth Factor 7 , Growth Substances/chemistry , Growth Substances/physiology , Heparin/chemistry , Humans , Light , Macromolecular Substances , Molecular Sequence Data , Peptide Fragments/chemistry , Protein Binding , Protein Structure, Tertiary , Receptor, Fibroblast Growth Factor, Type 2 , Receptors, Growth Factor/chemistry , Scattering, Radiation , Ultracentrifugation
11.
Proc Natl Acad Sci U S A ; 95(11): 6262-6, 1998 May 26.
Article in English | MEDLINE | ID: mdl-9600953

ABSTRACT

"Soft" and "hard" are the two main market classes of wheat (Triticum aestivum L.) and are distinguished by expression of the Hardness gene. Friabilin, a marker protein for grain softness (Ha), consists of two proteins, puroindoline a and b (pinA and pinB, respectively). We previously demonstrated that a glycine to serine mutation in pinB is linked inseparably to grain hardness. Here, we report that the pinB serine mutation is present in 9 of 13 additional randomly selected hard wheats and in none of 10 soft wheats. The four exceptional hard wheats not containing the serine mutation in pinB express no pinA, the remaining component of the marker protein friabilin. The absence of pinA protein was linked inseparably to grain hardness among 44 near-isogenic lines created between the soft variety Heron and the hard variety Falcon. Both pinA and pinB apparently are required for the expression of grain softness. The absence of pinA protein and transcript and a glycine-to-serine mutation in pinB are two highly conserved mutations associated with grain hardness, and these friabilin genes are the suggested tightly linked components of the Hardness gene. A previously described grain hardness related gene termed "GSP-1" (grain softness protein) is not controlled by chromosome 5D and is apparently not involved in grain hardness. The association of grain hardness with mutations in both pinA or pinB indicates that these two proteins alone may function together to effect grain softness. Elucidation of the molecular basis for grain hardness opens the way to understanding and eventually manipulating this wheat endosperm property.

12.
Protein Expr Purif ; 12(2): 189-200, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9518460

ABSTRACT

Keratinocyte growth factor (KGF) is a member of the fibroblast growth factor family that acts specifically on epithelial cells in a paracrine mode. We employed a mammalian expression system to synthesize recombinant human KGF and isolated two preparations, KGF-a and KGF-b, from medium conditioned by Chinese hamster ovary cells. On an SDS-PAGE gel, KGF-a migrates as two bands near 25-29 kDa and contains both N- and O-linked sugar moieties attached near the N-terminus. Detailed structural characterization confirms that KGF-a contains a single amino acid sequence predicted from cDNA sequence and the molecule has two intramolecular disulfide bridges, Cys1-Cys15 and Cys102-Cys106. An additional Cys at position 40 is free and resides in a solvent-inaccessible environment. Mass spectrometric analyses of KGF-a peptides verify the occurrence of several post-translational modifications in the molecule, including partial oxidation at Met28, partial sulfation at Tyr27, and glycosylation at Asn14 and Thr22. The Asn-linked carbohydrate structures are heterogeneous, which include biantennary, triantennary, and tetraantennary structures with none or up to four sialic acids attached to various structures, while the Thr-linked carbohydrates contain typical mucin-type structures. KGF-b is an N-terminally truncated form of KGF-a posttranslationally processed at Arg23 and is not glycosylated. Both KGF-a and KGF-b forms are capable of stimulating DNA synthesis in quiescent Balb/MK mouse epidermal keratinocytes.


Subject(s)
Fibroblast Growth Factors , Glycoproteins/isolation & purification , Glycoproteins/metabolism , Growth Substances/isolation & purification , Growth Substances/metabolism , Protein Processing, Post-Translational/genetics , Amidohydrolases/metabolism , Amino Acid Sequence , Animals , Base Sequence , Blotting, Western , CHO Cells , Carbohydrate Sequence , Cell Line , Chromatography, High Pressure Liquid , Cricetinae , DNA Primers/chemistry , Fibroblast Growth Factor 10 , Fibroblast Growth Factor 7 , Glycoproteins/chemistry , Glycoproteins/genetics , Growth Substances/chemistry , Growth Substances/genetics , Humans , Isomerism , Mass Spectrometry , Mice , Peptide Fragments/analysis , Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase , Polymerase Chain Reaction , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Serine Endopeptidases/metabolism
13.
Protein Sci ; 7(8): 1681-90, 1998 Aug.
Article in English | MEDLINE | ID: mdl-10082365

ABSTRACT

A comprehensive deletion, mutational, and structural analysis of the native recombinant keratinocyte growth factor (KGF) polypeptide has resulted in the identification of the amino acids responsible for its biological activity. One of these KGF mutants (delta23KGF-R144Q) has biological activity comparable to the native protein, and its crystal structure was determined by the multiple isomorphous replacement plus anomalous scattering method (MIRAS). The structure of KGF reveals that it folds into a beta-trefoil motif similar to other members of fibroblast growth factor (FGF) family whose structures have been resolved. This fold consists of 12 anti-parallel beta-strands in which three pairs of the strands form a six-stranded beta-barrel structure and the other three pairs of beta-strands cap the barrel with hairpin triplets forming a triangular array. KGF has 10 well-defined beta strands, which form five double-stranded anti-parallel beta-sheets. A sixth poorly defined beta-strand pair is in the loop between residues 133 and 144, and is defined by only a single hydrogen bond between the two strands. The KGF mutant has 10 additional ordered amino terminus residues (24-33) compared to the other FGF structures, which are important for biological activity. Based on mutagenesis, thermal stability, and structural data we postulate that residues TRP125, THR126, and His127 predominantly confer receptor binding specificity to KGF. Additionally, residues GLN152, GLN138, and THR42 are implicated in heparin binding. The increased thermal stability of delta23KGF-R144Q can structurally be explained by the additional formation of hydrogen bonds between the GLN side chain and a main-chain carbonyl on an adjoining loop. The correlation of the structure and biochemistry of KGF provides a framework for a rational design of this potentially important human therapeutic.


Subject(s)
Crystallography, X-Ray , DNA Mutational Analysis , Fibroblast Growth Factors , Growth Substances/chemistry , Amino Acid Sequence , Fibroblast Growth Factor 10 , Fibroblast Growth Factor 7 , Heparin/metabolism , Humans , Models, Molecular , Molecular Sequence Data , Protein Structure, Secondary , Sequence Homology, Amino Acid , Temperature
15.
Arch Biochem Biophys ; 332(1): 41-6, 1996 Aug 01.
Article in English | MEDLINE | ID: mdl-8806707

ABSTRACT

Binding of keratinocyte growth factor (KGF) with heparin (molecular weight of 5000) and dextran sulfate (molecular weight of 8000) was studied using an online monitoring of size-exclusion chromatography with light scattering, refractive index, and uv absorbance detectors. This technique allows the determination of the molecular weight of KGF eluting as complexes with the above polymers. When mixtures of KGF with heparin were injected into the column, two peaks of heparin/KGF complexes were observed. The first peak corresponded to, on average, 3.4 KGF per complex and the second peak to an average of about 2 KGF per complex. These results suggest that the heparin/ KGF complex is heterogeneous, consisting of 1,2,3, and 4 KGF molecules per complex. To calculate the number of heparin molecules in these complexes, the rate of disappearance of free KGF was determined as heparin was added. The average number of KGF bound to 1 mol of heparin was calculated to be about 2 mol, suggesting that only one heparin molecule is present in these complexes. The heparin binding of two KGF mutants, i.e., (C1, 15S)KGF (with substitutions of serine for cysteines 1 and 15) and d28KGF (lacking 28 N-terminal amino acid residues), was essentially identical to that of the native sequence KGF. A similar experiment was carried out for KGF binding to dextran sulfate. The molecular weight of the complex corresponded to 2 to 2.6 KGF molecules per complex. The rate of disappearance of free KGF as the dextran sulfate added showed 2-3 mol of KGF bound to 1 mol of dextran sulfate, consistent with the idea that the complex contains only 1 dextran sulfate molecule.


Subject(s)
Dextran Sulfate/metabolism , Fibroblast Growth Factors , Growth Substances/metabolism , Heparin/metabolism , Binding Sites , Dextran Sulfate/chemistry , Fibroblast Growth Factor 10 , Fibroblast Growth Factor 7 , Growth Substances/chemistry , Growth Substances/genetics , Heparin/chemistry , Humans , In Vitro Techniques , Kinetics , Macromolecular Substances , Molecular Weight , Mutation , Protein Binding , Protein Conformation , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism
17.
J Immunol ; 154(5): 2470-82, 1995 Mar 01.
Article in English | MEDLINE | ID: mdl-7868913

ABSTRACT

The rejection of pig proislet (islet precursor) xenografts in CBA/H mice is a CD4+ T cell-dependent process. The molecular mechanisms of xenograft rejection, xenograft survival during anti-CD4 mAb therapy and xenograft tolerance post-withdrawal of anti-CD4 mAb administration, were examined by using a semiquantitative PCR method. Temporal analysis of intragraft cytokine mRNA demonstrated a Th0-like pattern of expression (IL-2, IFN-gamma, IL-3, IL-4, IL-5, and IL-10) on day 4 of the acute xenograft rejection process. From day 5, however, only Th2-associated transcripts (IL-3, IL-4, IL-5, and IL-10) were enhanced in xenografts compared with isograft controls. Immunohistochemistry showed that the principal participants in the rejection infiltrate were CD4+ T cells and eosinophils, with smaller numbers of CD8+ T cells. In vivo depletion of CD4+ T cells prevented xenograft rejection but had minimal effect on the peak levels of IL-2, IFN-gamma, and IL-10 mRNA; in contrast, the enhanced expression of IL-3, IL-4, and IL-5 transcripts seen in rejecting xenografts was abrogated. This established a positive correlation between acute xenograft rejection, presence of CD4+ T cells, and enhanced intragraft expression of mRNA for the Th2-type cytokines IL-3, IL-4, and IL-5. In tolerant hosts, long-term proislet xenograft survival and function (> 190 days) was accompanied by intragraft expression of IL-2 and IL-10 mRNA; IFN-gamma, IL-3, IL-4, and IL-5 mRNA were either undetected or not enhanced. The induced rejection of long-term functioning xenografts (> 170 days) in nontolerant hosts resulted in selective enhancement of IL-4 transcript expression. This study suggests that Th2-like CD4+ T cells are differentially activated in response to xenoantigen and that xenograft tolerance is associated with lack of expression of the Th2 cytokine, IL-4.


Subject(s)
Cytokines/genetics , Fetal Tissue Transplantation/immunology , Graft Rejection/immunology , Islets of Langerhans Transplantation/immunology , Animals , Base Sequence , CD4-Positive T-Lymphocytes/immunology , DNA Primers/genetics , DNA, Complementary/genetics , Fetal Tissue Transplantation/pathology , Gene Expression , Graft Rejection/genetics , Graft Rejection/pathology , Immune Tolerance/genetics , Interleukin-2/genetics , Islets of Langerhans Transplantation/pathology , Male , Mice , Mice, Inbred CBA , Molecular Sequence Data , RNA, Messenger/genetics , RNA, Messenger/metabolism , Spleen/immunology , Swine , Transplantation, Heterologous
18.
Regul Pept ; 55(2): 179-88, 1995 Jan 26.
Article in English | MEDLINE | ID: mdl-7754104

ABSTRACT

Rats were given i.v., intranasal or intraperitoneal doses of CCK-8 (sulfated) labelled with 125I-labeled Bolton and Hunter reagent. Radioactivity was found mainly in the liver, kidney, and the intestinal contents. No radioactivity was detected in the brain. In animals dosed i.v., specific localization occurred in the tissue of the pyloric region of the stomach, and in the pancreas. Label persisted within the pyloric region of the stomach for longer than 30 min, in spite of the reported half-life of CCK-8 in plasma of approximately 1 min. Intranasal and intraperitoneal doses had limited bioavailability. The binding to the sites in the pyloric region of the stomach, which required systemic delivery, may have identified receptors associated with appetite control.


Subject(s)
Sincalide/analysis , Administration, Intranasal , Amino Acid Sequence , Animals , Autoradiography , Biological Availability , Brain/metabolism , Female , Frozen Sections , Injections, Intraperitoneal , Injections, Intravenous , Intestinal Mucosa/metabolism , Intestines/anatomy & histology , Iodine Isotopes , Isotope Labeling , Kidney/metabolism , Liver/metabolism , Molecular Sequence Data , Pancreas/anatomy & histology , Pancreas/metabolism , Pylorus/anatomy & histology , Pylorus/metabolism , Rats , Rats, Inbred F344 , Sincalide/administration & dosage , Sincalide/chemistry , Sincalide/pharmacokinetics , Tissue Distribution
19.
Toxicol Pathol ; 23(1): 26-33, 1995.
Article in English | MEDLINE | ID: mdl-7770697

ABSTRACT

A 90-day study was conducted to compare the effects of dietary administration of a food-grade white oil in female Fischer-344 (F-344) and Sprague-Dawley-derived (CRL:CD) rats. Animals were fed a low viscosity (15 mm2/sec at 40 degrees C) paraffinic white oil (designated as P 15[H]) at 0, 0.2, or 2.0% of the diet for 30, 61, or 92 days. There were no significant adverse clinical observations or unscheduled deaths. In the F-344 rats, occasional treatment-related changes were seen in hematology and clinical chemistry parameters. At necropsy, mesenteric lymph nodes were enlarged, and there was an increase in absolute and relative liver, mesenteric lymph node, and spleen weights as compared to controls. Histopathologic effects included hepatic and mesenteric lymph node microgranulomas and mesenteric lymph node histiocytosis. In CRL:CD rats, the only effects noted were accumulations of chronic inflammatory cells in the liver at the high dose only, without the formation of discrete microgranulomas. A dose-related increase in mineral hydrocarbon (MCH) material in the liver and mesenteric lymph nodes was observed in both F-344 and CRL:CD rats. Although increased, liver MhC content was significantly less (approximately 50%) in CRL:CD rats than the levels detected in the F-344 rats. Mesenteric lymph node MHC levels did not differ significantly between the strains. This study demonstrated strain differences among rats in histopathologic effects of white oil, with the CRL:CD rat essentially showing no response compared to the F-344 rat.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Liver/drug effects , Lymph Nodes/drug effects , Mineral Oil/toxicity , Animals , Blood Chemical Analysis , Chemical and Drug Induced Liver Injury , Dose-Response Relationship, Drug , Female , Granuloma/chemically induced , Granuloma/pathology , Histiocytosis/chemically induced , Histiocytosis/pathology , Liver/chemistry , Liver/pathology , Liver Diseases/pathology , Lymph Nodes/chemistry , Lymph Nodes/pathology , Mineral Oil/administration & dosage , Organ Size/drug effects , Rats , Rats, Inbred F344 , Rats, Sprague-Dawley
20.
J Oral Implantol ; 21(1): 8-18, 1995.
Article in English | MEDLINE | ID: mdl-7473873

ABSTRACT

This study conducted a longitudinal prospective clinical study of the single-crystal sapphire (Al2O3) cylindrical screw-shaped endosteal dental implant, and attempted to establish clinical parameters to evaluate implant success or failure. Twenty-eight mandibular implants (17 patients) were placed. After six weeks' healing, 23 implants in 15 patients served as distal abutments for fixed prostheses (baseline). Implants were evaluated for bleeding index, crevicular fluid volume index, plaque accumulation index, radiographic index, mobility index, and patient comfort. Any implant failing in three of these criteria or implants removed were judged as failures. After 10 years, of the 21 baseline implants recalled (two implants were lost to recall), 17 were fully functional, for an 81% success rate. The use of qualitative and quantitative clinical evaluation parameters as utilized in this study appears to be important and useful in assessments of the clinical serviceability of dental implants. These parameters can be used in human clinical trials as well as in experimental animal studies.


Subject(s)
Aluminum Oxide , Dental Implantation, Endosseous , Dental Implants , Analysis of Variance , Ceramics , Clinical Trials as Topic/standards , Dental Plaque Index , Dental Prosthesis Design , Dental Prosthesis Retention , Denture, Partial, Fixed , Gingival Crevicular Fluid/metabolism , Humans , Longitudinal Studies , Periodontal Index , Prospective Studies , Prosthesis Failure , Treatment Outcome
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