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Qualitative and quantitative analysis of rabbit's fat mesenchymal stem cells

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TLDR
The lipectomy of adipose panicule is a very satisfactory method to extract stem cells from fat, quantitatively and qualitatively.
Abstract
PURPOSE: To present an experimental model of qualitative and quantitative analysis of mesenchymal stem cells from fat of rabbits obtained by lipectomy. The fat could be a great source for obtaining mesenchymal stem cells and to create conditions for repairing injured tissues by bioengineering. METHODS: New Zealand rabbits (n= 10) adipose panicle (2-3 cm) were removed by lipectomy, fragmented and washed with PBS and enzymatically dissociated with trypsin/EDTA. Lately, these cells were incubated in culture medium DMEM and after 20 days, was performed quantitative analysis of the accession of first and second mesenchymal cells in cell culture bottles. RESULTS: The fat total cells (CTF) were 1.62 x106 cells/mL and presented 98% of viability. These cells were taken for cultivation and after 20 days were counted 2.88 x106 cells/mL MSC. The same was done and after 20 days we quantified 4.28 x106 cells/mL MSC. CONCLUSION: The lipectomy of adipose panicule is a very satisfactory method to extract stem cells from fat, quantitatively and qualitatively.

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Exosomes in mesenchymal stem cells, a new therapeutic strategy for cardiovascular diseases?

TL;DR: Recent advances about the role of exosome in MSCs therapy for CVDs are summarized, and exosomes are discussed as a novel approach in the treatment ofCVDs in the future.
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A safety study on intrathecal delivery of autologous mesenchymal stromal cells in rabbits directly supporting Phase I human trials.

TL;DR: This preclinical study evaluated the safety of intrathecal autologous MSCs in a rabbit model and found them to be safe and effective in treating neurodegenerative diseases.
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Adipose mesenchymal stem cells associated with xenograft in a guided bone regeneration model: a histomorphometric study in rabbit calvaria.

TL;DR: It is suggested that the association of mesenchymal stem cells derived from adipose tissue with a xenogenic bone graft was capable of promoting better bone regeneration compared with the use of a xenograft alone.
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Phenotype and multipotency of rabbit ( Oryctolagus cuniculus ) amniotic stem cells

TL;DR: It is demonstrated that multipotent mesenchymal stem cells can be obtained from the rabbit amniotic membrane and had the capacity to be induced to differentiate into osteogenic, adipogenic and chondrogenic lineages.
References
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Journal ArticleDOI

Multilineage cells from human adipose tissue: implications for cell-based therapies.

TL;DR: The data support the hypothesis that a human lipoaspirate contains multipotent cells and may represent an alternative stem cell source to bone marrow-derived MSCs.
Journal ArticleDOI

Adipose Tissue as an Endocrine Organ

TL;DR: An overview of the endocrine functions of adipose tissue can be found in this paper, where the authors highlight the adverse metabolic consequences of both adipose excess and deficiency, and propose a more rational therapy for these increasingly prevalent disorders.
Journal ArticleDOI

The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells.

TL;DR: The linear increase in the number of colonies with increasing numbers of explanted cells and the distribution of male and female cells in mixed cultures support the view that fibroblast colonies are clones.
Journal ArticleDOI

Understanding Adipocyte Differentiation

TL;DR: Characterization of regulatory regions of adipose-specific genes has led to the identification of the transcription factors peroxisome proliferator-activated receptor-gamma and CCAAT/enhancer binding protein (C/EBP), which play a key role in the complex transcriptional cascade during adipocyte differentiation.
Journal ArticleDOI

Adipose Tissue as an Endocrine Organ

TL;DR: The discovery of leptin in the mid-1990s has focused attention on the role of proteins secreted by adipose tissue, which is also involved in the regulation of neuroendocrine and immune function and the metabolic and cardiovascular complications associated with obesity.
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How much time does it take for fat cells to shrink?

The fat total cells (CTF) were 1.62 x10(6) cells/mL and presented 98% of viability.