ABSTRACT
The integrin alpha9 subunit forms a single heterodimer, alpha9beta1. The alpha9 subunit is most closely related to the alpha4 subunit, and like alpha4 integrins, alpha9beta1 plays an important role in leukocyte migration. The alpha4 cytoplasmic domain preferentially enhances cell migration and inhibits cell spreading, effects that depend on interaction with the adaptor protein, paxillin. To determine whether the alpha9 cytoplasmic domain has similar effects, a series of chimeric and deleted alpha9 constructs were expressed in Chinese hamster ovary cells and tested for their effects on migration and spreading on an alpha9beta1-specific ligand. Like alpha4, the alpha9 cytoplasmic domain enhanced cell migration and inhibited cell spreading. Paxillin also specifically bound the alpha9 cytoplasmic domain and to a similar level as alpha4. In paxillin(-/-) cells, alpha9 failed to inhibit cell spreading as expected but surprisingly still enhanced cell migration. Further, mutations that abolished the alpha9-paxillin interaction prevented alpha9 from inhibiting cell spreading but had no effect on alpha9-dependent cell migration. These findings suggest that the mechanisms by which the cytoplasmic domains of integrin alpha subunits enhance migration and inhibit cell spreading are distinct and that the alpha9 and alpha4 cytoplasmic domains, despite sequence and functional similarities, enhance cell migration by different intracellular signaling pathways.
Subject(s)
Cell Movement/physiology , Cytoplasm/metabolism , Cytoskeletal Proteins/metabolism , Integrin alpha Chains , Integrins/metabolism , Phosphoproteins/metabolism , Amino Acid Motifs/physiology , Animals , CHO Cells , Cell Adhesion/drug effects , Cell Adhesion/physiology , Cell Movement/drug effects , Cricetinae , Cytoskeletal Proteins/pharmacology , Focal Adhesions/physiology , Integrins/genetics , Paxillin , Phosphoproteins/pharmacology , Point Mutation/genetics , Protein Binding/physiology , Protein Structure, Tertiary/physiology , Recombinant Fusion Proteins/metabolism , Recombinant Proteins/metabolismABSTRACT
To identify factors regulating neurogenesis and programmed cell death in mouse olfactory epithelium (OE), and to determine the mechanisms by which these factors act, we have studied mouse OE using two major experimental paradigms: tissue culture of embryonic OE and cell types isolated from it; and ablation of the olfactory bulb ('bulbectomy') of adult mice, a procedure that induces programmed cell death of olfactory receptor neurons (ORNS) and a subsequent surge of neurogenesis in the OE in vivo. Such experiments have been used to characterize the cellular stages in the ORN lineage, leading to the realization that there are at least two distinct stages of proliferating neuronal progenitor cells interposed between the ORN and the stem cell that ultimately gives rise to it. The identification of a number of different factors that act to regulate proliferation and survival of ORNs and progenitor cells suggests that these multiple cell stages may each serve as a control point at which neuron number in the OE is regulated. Our recent studies of neuronal colony-forming progenitors (putative stem cells) of the OE suggest that even these cells, at the earliest stage in the ORN lineage so far identified, are subject to such regulation: if colony-forming progenitors are cultured in the presence of a large excess of differentiated ORNs, then the production of new neurons by progenitors is dramatically inhibited. This result suggests that differentiated ORNs produce a signal that feeds back to inhibit neurogenesis by their own progenitors, and provides a possible explanation for the observation that ORN death, consequent to bulbectomy, results in increased neurogenesis in the OE in vivo: death of ORNs may release neuronal progenitor cells from this inhibitory signal, produced by the differentiated ORNs that lie near them in the OE. Our current experiments are directed toward identifying the molecular basis of this inhibitory signal, and the cellular mechanism(s) by which it acts.
Subject(s)
Apoptosis , Epithelial Cells/pathology , Olfactory Receptor Neurons/cytology , Animals , Cell Differentiation , Cell Lineage/physiology , Mice , Olfactory Mucosa/pathology , Olfactory Mucosa/physiology , Paracrine CommunicationABSTRACT
Human papillomaviruses (HPVs) reproduce only in differentiated squamous epithelia. Viral transcription is rather restricted in basal strata but increases dramatically in the spinous cells. Inopportune viral oncoprotein expression in the basal reserve cells can lead to dysplasias and carcinomas. Until now all studies to identify transcription factor binding sites within the upstream regulatory region (URR) that controls the expression of the oncogene have been conducted in proliferating cell cultures. We report the establishment of a reproducible and convenient system to examine cis elements important for differentiation-dependent transcriptional regulation. The bacterial lacZ gene under the control of the HPV URR-E6 promoter was transduced into primary human keratinocytes from neonatal foreskin by using high titer recombinant retroviruses. Acutely infected PHKs were then grown into stratified and differentiated epithelium on collagen rafts. lacZ expression was almost entirely restricted to the spinous cells, indicating that promoter activity was differentiation dependent, as seen in vivo. Using this system, we initiated a mutational analysis of previously identified promoter and enhancer elements within the HPV-18 URR. Three categories of mutation were observed: those that caused severe, moderate, or very small reduction in lacZ expressions. The results show both similarities and differences to previously published and present studies in proliferating primary human keratinocytes in monolayer cultures or in immortalized or transformed cell lines. This system is applicable to study both host and viral promoters that require squamous differentiation for their activity.
Subject(s)
DNA-Binding Proteins , Enhancer Elements, Genetic/genetics , Gene Expression Regulation, Viral/genetics , Keratinocytes/physiology , Papillomaviridae/genetics , Cell Differentiation , Cells, Cultured , DNA Mutational Analysis , Epithelial Cells , Genetic Vectors/genetics , Humans , Infant, Newborn , Keratinocytes/cytology , Moloney murine leukemia virus/genetics , Oncogene Proteins, Viral/genetics , Point Mutation , Promoter Regions, Genetic/genetics , Skin/cytologyABSTRACT
Alcohol dehydrogenase (E. C. 1.1.1.1) from Thermoanaerobium brockii at 25 degrees C and at 65 degrees C is more active with secondary than primary alcohols. The enzyme utilizes NADP and NADPH as cosubstrates better than NAD and NADH. The maximum velocities (V(m)) for secondary alcohols at 65 degrees C are 10 to 100 times higher than those at 25 degrees C, whereas the K(m) values are more comparable.At both 25 degrees C and 65 degrees C the substrate analogue 1,1,1,3,3,3-hexafluoro-2-propanol inhibited the oxidation of alcohol competitively with respect to cyclopentanol, and uncompetitively with respect to NADP. Dimethylsulfoxide inhibited the reduction of cyclopentanone competitively with respect to cyclopentanone, and uncompetitively with respect to NADPH. As a product inhibitor, NADP was competitive with respect to NADPH. These results demonstrate that the enzyme binds the nucleotide and then the alcohol or ketone to form a ternary complex which is converted to a product ternary complex that releases product and nucleotide in that order.At 25 degrees C, all aldehydes and ketones examined inhibited the enzyme at concentrations above their Michaelis constants. The substrate inhibition by cyclopentanone was incomplete, and it was uncompetitive with respect to NADPH. Furthermore, cyclopentanone as a product inhibitor showed intercept-linear, slope-parabolic inhibition with respect to cyclopentanol. These results indicate that cyclopentanone binds to the enzyme-NADP complex at high concentrations. The resulting ternary complex slowly dissociates NADP and cyclopentanone.At 65 degrees C, all of the secondary alcohols, with the exception of cyclohexanol, show substrate activation at high concentration. Experiments in which NADP was the variable substrate and cyclopentanol as the constant-variable substrate over a wide range of concentrations gave double reciprocal plots in which the intercepts showed substrate activation and the slopes showed substrate inhibition. These results indicate that the secondary alcohols bind to the enzyme-NADPH complex at high concentrations and that the resulting ternary complex dissociates NADPH faster than the enzyme-NADPH complex.