scholarly journals ПОРІВНЯЛЬНА ХАРАКТЕРИСТИКА ФЕНОТИПОВИХ ЗМІН КУЛЬТУР КЛІТИН ЖИРОВОЇ ТКАНИНИ ТА КІСТКОВОГО МОЗКУ В ПРОЦЕСІ КУЛЬТИВУВАННЯ

2017 ◽  
pp. 113-119 ◽  
Author(s):  
В. В. Ковпак ◽  
О. С. Ковпак
Keyword(s):  
Bone Marrow ◽  
Adipose Tissue ◽  
Cell Cultures ◽  
Bone Marrow Cells ◽  
Primary Cultures ◽  
Tissue Cell ◽  
Adipose Tissue Cell ◽  
Polygonal Shape ◽  
Adipose Tissue Cells ◽  
Number Of Cells

У статті описані дані щодо зміни фенотипу культур клітин жирової тканини (ККЖТ) та кісткового мозку (КККМ) у процесі культивування. Дослідження первинних культур клітин кісткового мозку та жирової тканини щура показали, що вони морфологічно гетерогенні, у їх склад входили: невелика кількість клітин полігональної форми, а основну масу складали фібробластоподібні. За подальшого культивування відмічали процес переходу від гетерогенних культур на нульовому  пасажі до найбільш гомогенних у кінці дослідження. Нами були відмічені відмінності у імунофенотипі культур клітин кісткового мозку та жирової тканини, які не зникали з пасажами. This article describes the changes in phenotype of cultures of adipose tissue cells (ATCC) and bone marrow cells (BMCC) in the process of cultivation. Study of primary cultures of cells of the bone marrow and adipose tissue of rat has shown that they are morphologically heterogeneous, they included: a small number of cells of polygonal shape, and the bulk was fìbroblast-like cells. Process of transition from the heterogeneous cultures at zero passaging to the most homogeneous at the end of the study was noted during further cultivation. We noted differences in immunophenotype of bone marrow and adipose tissue cell cultures that did not disappear with passaging.

Hyperinsulinemia in obesity: Importance of adipose tissue cell size

1983 ◽  
Vol 96 (6) ◽  
pp. 1689-1691
Author(s):  
U. Julius ◽  
M. Weck ◽  
W. Leonhardt ◽  
H. Schneider ◽  
K. Schollberg ◽  
...  
Keyword(s):  
Adipose Tissue ◽  
Cell Size ◽  
Tissue Cell ◽  
Adipose Tissue Cell

scholarly journals Assessing the Contribution of Relative Macrophage Frequencies to Subcutaneous Adipose Tissue

2021 ◽  
Vol 8 ◽  
Author(s):  
Marianthi Kalafati ◽  
Michael Lenz ◽  
Gökhan Ertaylan ◽  
Ilja C. W. Arts ◽  
Chris T. Evelo ◽  
...  
Keyword(s):  
Gene Expression ◽  
Adipose Tissue ◽  
Subcutaneous Adipose Tissue ◽  
Tissue Cell ◽  
Cell Type ◽  
Expression Of Genes ◽  
Cell Type Composition ◽  
Type Composition ◽  
Adipose Tissue Cell ◽  
Subcutaneous Adipose

Background: Macrophages play an important role in regulating adipose tissue function, while their frequencies in adipose tissue vary between individuals. Adipose tissue infiltration by high frequencies of macrophages has been linked to changes in adipokine levels and low-grade inflammation, frequently associated with the progression of obesity. The objective of this project was to assess the contribution of relative macrophage frequencies to the overall subcutaneous adipose tissue gene expression using publicly available datasets.Methods: Seven publicly available microarray gene expression datasets from human subcutaneous adipose tissue biopsies (n = 519) were used together with TissueDecoder to determine the adipose tissue cell-type composition of each sample. We divided the subjects in four groups based on their relative macrophage frequencies. Differential gene expression analysis between the high and low relative macrophage frequencies groups was performed, adjusting for sex and study. Finally, biological processes were identified using pathway enrichment and network analysis.Results: We observed lower frequencies of adipocytes and higher frequencies of adipose stem cells in individuals characterized by high macrophage frequencies. We additionally studied whether, within subcutaneous adipose tissue, interindividual differences in the relative frequencies of macrophages were reflected in transcriptional differences in metabolic and inflammatory pathways. Adipose tissue of individuals with high macrophage frequencies had a higher expression of genes involved in complement activation, chemotaxis, focal adhesion, and oxidative stress. Similarly, we observed a lower expression of genes involved in lipid metabolism, fatty acid synthesis, and oxidation and mitochondrial respiration.Conclusion: We present an approach that combines publicly available subcutaneous adipose tissue gene expression datasets with a deconvolution algorithm to calculate subcutaneous adipose tissue cell-type composition. The results showed the expected increased inflammation gene expression profile accompanied by decreased gene expression in pathways related to lipid metabolism and mitochondrial respiration in subcutaneous adipose tissue in individuals characterized by high macrophage frequencies. This approach demonstrates the hidden strength of reusing publicly available data to gain cell-type-specific insights into adipose tissue function.

Hypercholesterolemia of total starvation: its mechanism via tissue mobilization of cholesterol

1975 ◽  
Vol 229 (2) ◽  
pp. 365-369 ◽  
Author(s):  
JC Swaner ◽  
WE Connor
Keyword(s):  
Adipose Tissue ◽  
Cholesterol Metabolism ◽  
Plasma Cholesterol ◽  
Specific Radioactivity ◽  
Cholesterol Content ◽  
Cholesterol Concentration ◽  
Tissue Cell ◽  
Adipose Tissue Cell ◽  
Total Starvation ◽  
Linear Decay

After the establishment of a relatively linear decay curve for plasma [4-14C]cholesterol, rabbits were starved for 26-32 days. The plasma cholesterol concentration increased 400% during starvation. Concurrently, the plasma triglyceride level declined by 50%. While the plasma cholesterol was rising, the cholesterol specific radioactivity of the plasma remained unchanged in starved animals, but in control animals the plasma cholesterol specific radioactivity declined substantially. The cholesterol content of the liver and adipose tissue increased with starvation. The cholesterol specific radioactivities relative to plasma for adipose tissue were lower in the starved animals versus controls. These results support the hypothesis that cholesterol stored in the lipid droplet of the adipose tissue cell is released into plasma and is the chief source of the hypercholesterolemia observed during complete caloric starvation. Cholesterol metabolism in the starved animal can be depicted as a virtually closed system in both the input from biosynthesis and diet being low or zero and the output likewise being close to zero.

scholarly journals The action of bryostatin on normal human hematopoietic progenitors is mediated by accessory cell release of growth factors

Blood ◽  
1990 ◽  
Vol 76 (4) ◽  
pp. 716-720 ◽  
Author(s):  
SJ Sharkis ◽  
RJ Jones ◽  
ML Bellis ◽  
GD Demetri ◽  
JD Griffin ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Growth Factors ◽  
Single Cell ◽  
Cell Cultures ◽  
Bone Marrow Cells ◽  
Human Bone ◽  
Human Bone Marrow ◽  
Accessory Cell ◽  
Bryostatin 1 ◽  
Gm Csf

Abstract Since enrichment of human bone-marrow hematopoietic progenitors is becoming more feasible and since purified growth factors are now available, we sought to study the action of growth factors on CD34- positive enriched cultures of human bone-marrow cells. We tested the effect of recombinant human (rh) granulocyte-macrophage colony- stimulating factor (GM-CSF), rh interleukin-3 (IL-3), or a unique biologic response modifier, bryostatin 1, on the growth of purified CD34 cells obtained by limiting dilution in single-cell cultures. We have shown previously that bryostatin 1 stimulates both myeloid and erythroid progenitors of human origin in vitro. In this study both IL-3 and GM-CSF supported colony formation from 500, 100, or single-cell cultures at equivalent plating efficiences, suggesting a direct action of these factors on hematopoietic cell growth. Conversely, bryostatin 1 did not support the growth of CD34 cells in single-cell cultures, and the cloning efficiency increased with increasing the number of cells in the culture. To test whether the indirect action of bryostatin 1 might be mediated through the production of growth factors by accessory cells, studies were performed using antibodies directed against human IL-3 and GM-CSF in culture with bryostatin 1 and normal human bone- marrow cells. Results are consistent with the hypothesis that bryostatin 1 could have a stimulatory effect on the accessory cell populations to produce either IL-3 or GM-CSF. Further support for this notion was obtained by demonstrating that T cells, which are cells known to be able to produce IL-3 and GM-CSF, are stimulated by bryostatin 1 to express messenger RNA (mRNA) for specific growth factors, including GM-CSF. These results provide further support that bryostatin 1 may be a useful clinical agent to stimulate hematopoiesis in vivo.

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