scholarly journals Histoplasma capsulatum modulates the acidification of phagolysosomes.

1993 ◽  
Vol 177 (6) ◽  
pp. 1605-1611 ◽  
Author(s):  
L G Eissenberg ◽  
W E Goldman ◽  
P H Schlesinger

The phagolysosome is perhaps the most effective antimicrobial site within macrophages due both to its acidity and to its variety of hydrolytic enzymes. Few species of pathogens survive and multiply in these vesicles. However, one strategy for microbial survival would be to induce a higher pH within these organelles, thus interfering with the activity of many lysosomal enzymes. Altering the intravesicular milieu might also profoundly influence antigen processing, antimicrobial drug delivery, and drug activity. Here we report the first example of an organism proliferating within phagolysosomes that maintain a relatively neutral pH for a sustained period of time. We inoculated P388D1 macrophages with fluorescein isothiocyanate (FITC)-labeled Histoplasma capsulatum or zymosan. Using the ratio of fluorescence excitations at 495 and 450 nm, we determined that vesicles containing either virulent or avirulent FITC-labeled H. capsulatum yeasts had a pH one to two units higher than vesicles containing either zymosan or methanol-killed H. capsulatum. The difference in pH remained stable for at least 5.5 h postinoculation. Longer-term studies using cells preincubated with acridine orange indicated that phagolysosomes containing live Histoplasma continued to maintain a relatively neutral pH for at least 30 h. Many agents raise the pH of multiple vesicles within the same cell. In contrast, H. capsulatum affects only the phagolysosome in which it is located; during coinoculation of cells with unlabeled Histoplasma and labeled zymosan, organelles containing zymosan still acidified normally. Similarly, unlabeled zymosan had no influence on the elevated pH of vesicles housing labeled Histoplasma. Thus, zymosan and Histoplasma were segregated into separate phagolysosomes that responded independently to their phagocytized contents. This localized effect might reflect an intrinsic difference between phagosomes housing the two particle types, active buffering by the microbe, or altered ion transport across the phagolysosomal membrane such that acidification is inhibited.

1977 ◽  
Vol 25 (7) ◽  
pp. 875-880 ◽  
Author(s):  
Z Darzynkiewicz ◽  
F Traganos ◽  
T Sharpless ◽  
M R Melamed

Cells in mitosis may be distinguished from interphase cells based on difference in chromatin structure as revealed by two different methods of staining with acridine orange. In the first method, cells are heated and then stained at neutral pH; the difference in stainability between mitotic and interphase cells reflects the difference in the extent of deoxyribonucleic acid denatured by heat in these cells. At a given temperature the deoxyribonucleic acid of the mitotic cell appears to be more extensively denatured than that of the interphase cell. In the second method, cells are treated with buffer at pH 1.5 (1.3 to 1.9) and then stained at pH 2.6 (2.3 to 2.9). The mechanisms involved in the differential stainability of interphase versus mitotic cells at that low pH are currently under investigation. In both methods, in addition to enumerating cells in mitosis, it is possible to quantitate cells in G1, S and G2 phases of the cell cycle.


2019 ◽  
Vol 42 (5) ◽  
pp. 1328-1341 ◽  
Author(s):  
Weifang Hu ◽  
Linhai Zhang ◽  
Derrick Y. F. Lai ◽  
Jintao Gao ◽  
Zhigao Sun ◽  
...  

2011 ◽  
Vol 26 (6) ◽  
pp. 619-627 ◽  
Author(s):  
V.H. Pereira ◽  
A.J. Salgado ◽  
J.M. Oliveira ◽  
S.R. Cerqueira ◽  
A.M. Frias ◽  
...  

Carboxymethylchitosan/poly(amidoamine) (CMCht/PAMAM) dendrimer nanoparticles, comprised of a PAMAM dendrimer core grafted with chains of CMCht, have recently been proposed for intracellular drug delivery. In previous reports, these nanoparticles had lower levels of cytotoxicity when compared with traditional dendrimers. In this study, the short-term in vivo biodistribution of fluorescein isothiocyanate (FITC)-labeled CMCht/PAMAM dendrimer nanoparticles after intravenous (IV) injections in Wistar Han rats was determined. The brain, liver, kidney, and lung were collected at 24, 48, and 72 h after injection and stained with phalloidin–tetramethylrhodamine isothiocyanate (TRITC, red) and 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI, blue) to trace the nanoparticles within these tissues. The liver, kidney, and lung were also stained for hematoxylin and eosin to assess any morphological alterations of these organs. CMCht/PAMAM dendrimer nanoparticles were observed within the vascular space and parenchyma of liver, kidney, and lung and in the choroid plexus, after each injection period. No particles were observed in the brain parenchyma, nor any apparent deleterious histological changes were observed within these organs. The CMCht/PAMAM dendrimer nanoparticles were stable in circulation for a period of up to 72 h, targeting the main organs/systems through internalization by the cells present in their parenchyma. These results provide positive indicators to their potential use in the future as intracellular drug delivery systems.


Author(s):  
Daxiong He ◽  
Weixing Chen ◽  
Jingli Luo ◽  
Fraser King ◽  
Tom Jack ◽  
...  

This research has focused on the effect of surface roughness and surface scratch orientation on the development of neutral pH SCC on pipeline steels. The susceptibility to neutral pH SCC was assessed in this study using slow strain rate testing on X-65 line pipe steel. The surfaces of the test samples were ground using either #240 or #600 sandpaper to introduce different scratch roughness. Scratches were produced with an orientation parallel, perpendicular and inclined at 45° to the loading direction, respectively. The test samples were exposed to a synthetic neutral pH ground water at both open circuit potential (OCP) and −800 mV (SCE). It has been found that the reduction in ductility due to a near neutral pH environment was more than 20% larger for the specimens with perpendicular scratches than those with parallel scratches, either at OCP or −800 mV (SCE). Roughness appeared to have little effect on the ductility of the specimen with parallel scratches. However, it has some effect on the sample with perpendicular scratches. For these samples, a finer scratch caused more reduction in ductility than the rougher scratches, particularly under cathodically protected conditions. The reduction in ductility for the specimen with scratches 45° inclined to stress axis was in between those with parallel and perpendicular scratches. The difference in ductility arising from scratch roughness and orientation was consistent with the observation of the surface conditions after test. For samples with perpendicular and angle scratches, cracks were seen to coincide with scratch lines. For those with parallel scratches, only short cracks developed in a direction approximately 45° to the stress axis. Mechanisms concerning this scratch-facilitated crack formation are discussed.


1979 ◽  
Vol 27 (1) ◽  
pp. 478-485 ◽  
Author(s):  
Z Darzynkiewicz ◽  
F Traganos ◽  
M Andreeff ◽  
T Sharpless ◽  
M R Melamed

The properties of DNA in situ as reflected by its staining with acridine orange are different in quiescent nonstimulated lymphocytes as compared with interphase lymphocytes that have entered the cell cycle after stimulation by mitogens. The difference is seen after cell treatment with buffers at pH 1.5 (1.3-1.9 range) followed by staining with acridine orange at pH 2.6 (2.3-2.9). Under these conditions the red metachromatic fluorescence of the acridine orange-DNA complex is higher in quiescent cells than in the cycling lymphocytes while the orthochromatic green fluorescence is higher in the cycling, interphase cells. The results suggest that DNA in condensed chromatin of quiescent lymphocytes (as in metaphase chromosomes) is more sensitive to acid-denaturation than DNA in dispersed chromatin of the cycling interphase cells. The phenomenon is used for flow cytometric differentiation between G0 and G1 cells and between G2 and M cells. In contrast to normal lymphocytes the method applied to neoplastic cells indicates the presence of cell subpopulations with condensed chromatin but with DNA content characteristic not only of G1 but also of S and G2 cells. The possibility that these cells represent quiescent (resting) subpopulations, arrested in G1, S and/or G2, is discussed.


2014 ◽  
Vol 1 (1) ◽  
Author(s):  
Fransisca Leonard ◽  
Katherine Margulis ◽  
Xuewu Liu ◽  
Srimeenakshi Srinivasan ◽  
Shlomo Magdassi ◽  
...  

AbstractEnsuring drug loading efficiency and consistency is one of the most critical stages in engineering drug delivery vectors based on porous materials. Here we propose a technique to significantly enhance the effciency of loading by employing simple and widely available methods: applying low pressure with and without centrifugation. Our results point toward the advantages of the proposed method over the passive loading, especially when the difference between the dimensions of loaded materials and the pore diameter is small, an increase of up to 20-fold can be observed. The technique described in this study can be used for efficient and reproducible loading of porous materials with therapeutic molecules, nanoparticles and contrast imaging agents for biomedical applications.


Pharmaceutics ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 209 ◽  
Author(s):  
Ajeesh Chandrasekharan ◽  
Young Jun Hwang ◽  
Keum-Yong Seong ◽  
Samdae Park ◽  
Sodam Kim ◽  
...  

Chitosan has been widely used as a nature-derived polymeric biomaterial due to its high biocompatibility and abundance. However, poor solubility in aqueous solutions of neutral pH and multiple fabrication steps for the molding process limit its application to microneedle technology as a drug delivery carrier. Here, we present a facile method to prepare water-soluble chitosan and its application for sustained transdermal drug delivery. The water-soluble chitosan was prepared by acid hydrolysis using trifluoroacetic acid followed by dialysis in 0.1 M NaCl solutions. We successfully fabricated bullet-shaped microneedle (MN) arrays by the single molding process with neutral aqueous chitosan solutions (pH 6.0). The chitosan MN showed sufficient mechanical properties for skin insertion and, interestingly, exhibited slow dissolving behavior in wet conditions, possibly resulting from a physical crosslinking of chitosan chains. Chitosan MN patches loading rhodamine B, a model hydrophilic drug, showed prolonged release kinetics in the course of the dissolving process for more than 72 h and they were found to be biocompatible to use. Since the water-soluble chitosan can be used for MN fabrication in the mild conditions (neutral pH and 25 °C) required for the loading of bioactive agents such as proteins and achieve a prolonged release, this biocompatible chitosan MN would be suitable for sustained transdermal drug delivery of a diverse range of drugs.


2008 ◽  
Vol 7 (7) ◽  
pp. 1109-1117 ◽  
Author(s):  
Li Shi ◽  
Priscila C. Albuquerque ◽  
Eszter Lazar-Molnar ◽  
Xintao Wang ◽  
Laura Santambrogio ◽  
...  

ABSTRACT Monoclonal antibodies (MAbs) to a cell surface histone on Histoplasma capsulatum modify murine infection and decrease the growth of H. capsulatum within macrophages. Without the MAbs, H. capsulatum survives within macrophages by modifying the intraphagosomal environment. In the present study, we aimed to analyze the affects of a MAb on macrophage phagosomes. Using transmission electron and fluorescence microscopy, we showed that phagosome activation and maturation are significantly greater when H. capsulatum yeast are opsonized with MAb. The MAb reduced the ability of the organism to regulate the phagosomal pH. Additionally, increased antigen processing and reduced negative costimulation occur in macrophages that phagocytose yeast cells opsonized with MAb, resulting in more-efficient T-cell activation. The MAb alters the intracellular fate of H. capsulatum by affecting the ability of the fungus to regulate the milieu of the phagosome.


1969 ◽  
Vol 5 (1) ◽  
pp. 57-63
Author(s):  
SHIRLEY E. HAWKINS ◽  
LESLEY R.WILLIS

The growth of Amoeba proteus (T1P) and Amoeba discoides (T1) in the trypanocidal phenanthridlnium, dimidium bromide was examined. At concentrations of drug between 2 and 4 µg/ml, A. proteus divided twice before inhibition and death. A. discoides was able to undergo an additional cycle of division before death. At other concentrations there were no differences in their response. Heterotransfers between these strains resembled A. discoides, both dividing three times before death. Examination of clones derived from the micro-injection of small quantities of A. discoides cytoplasm into A. proteus showed that the ability to divide additionally in dimidium bromide could be transferred. Some other strains of A. proteus (DP, T4P) also resembled A. discoides in their response. Cells of all the strains used were treated with acridine orange and observed under the fluorescence microscope for the presence of DNA- and RNA-containing cytoplasmic ‘bodies’. All strains able to undergo an additional division cycle also possessed cytoplasmic DNAcontaining bodies. The converse was not 100%, but this may be due to a quantitative difference in the number of DNA-containing bodies in the cytoplasm. It is proposed that the difference in response to dimidium bromide observed in A. proteus and A. discoides may be associated with the presence of DNA- and RNA-containing bodies in the cytoplasm of A. discoides.


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