<meta charset="utf8"></head><body>SATMVEC umane: isolamento e studi cross-talk con gli adipociti

<ol>
	<li>Bierhansl, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Central+role+of+metabolism+in+endothelial+cell+function+and+vascular+disease.">Central role of metabolism in endothelial cell function and vascular disease.</a> Physiology. 32 (2), 126-140 (2017).</li><li>Aird, W. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endothelial+cell+heterogeneity.">Endothelial cell heterogeneity.</a> Cold Spring Harb Perspect Med. 2 (1), a006429 (2012).</li><li>Rajendran, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+vascular+endothelium+and+human+diseases.">The vascular endothelium and human diseases.</a> Int J Biol Sci. 9 (10), 1057-1069 (2013).</li><li>Brown, O. I., Bridge, K., Kearney, M. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nicotinamide+adenine+dinucleotide+phosphate+oxidases+in+glucose+homeostasis+and+diabetes-related+endothelial+cell+dysfunction.">Nicotinamide adenine dinucleotide phosphate oxidases in glucose homeostasis and diabetes-related endothelial cell dysfunction.</a> Cells. 10 (9), 2315 (2021).</li><li>Luk, C., Haywood, N. J., Bridge, K. I., Kearney, M. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Paracrine+role+of+the+endothelium+in+metabolic+homeostasis+in+health+and+nutrient+excess.">Paracrine role of the endothelium in metabolic homeostasis in health and nutrient excess.</a> Front Cardiovasc Med. 26 (9), 882923 (2022).</li><li>. Click-iT EdU Imaging Kits Available from: <a target="_blank" href="https://www.thermofisher.com/document-connect/document-connect.html?url=https://assets.thermofisher.com/TFS-Assets%2FLSG%2Fmanuals%2Fmp10338.pdf">https://www.thermofisher.com/document-connect/document-connect.html?url=https://assets.thermofisher.com/TFS-Assets%2FLSG%2Fmanuals%2Fmp10338.pdf</a> (2024)</li><li>Bou&#239;s, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endothelium+in+vitro:+A+review+of+human+vascular+endothelial+cell+lines+for+blood+vessel-related+research.">Endothelium in vitro: A review of human vascular endothelial cell lines for blood vessel-related research.</a> Angiogenesis. 4 (2), 91-102 (2001).</li><li>Ades, E. W., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=HMEC-1:+establishment+of+an+immortalized+human+microvascular+endothelial+cell+line.">HMEC-1: establishment of an immortalized human microvascular endothelial cell line.</a> J Invest Dermatol. 99 (6), 683-690 (1992).</li><li>Chi, J. T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endothelial+cell+diversity+revealed+by+global+expression+profiling.">Endothelial cell diversity revealed by global expression profiling.</a> Proc Natl Acad Sci U S A. 100 (19), 10623-10628 (2003).</li><li>Brignole, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=213+ESC+Guidelines+on+cardiac+pacing+and+cardiac+resynchronization+therapy.">213 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy.</a> Eur Heart J. 34 (29), 2281-2329 (2013).</li><li>Greenspon, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Trends+in+permanent+pacemaker+implantation+in+the+United+States+from+1993+to+2009:+Increasing+complexity+of+patients+and+procedures.">Trends in permanent pacemaker implantation in the United States from 1993 to 2009: Increasing complexity of patients and procedures.</a> J Am Coll Cardiol. 60 (16), 1540-1545 (2012).</li><li>Mendis, S. A., Alwan, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Prioritized Research Agenda for Prevention and Control of Noncommunicable Diseases. , (2011).</li><li>Brown, O. I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Relationship+among+diabetes,+obesity,+and+cardiovascular+disease+phenotypes:+A+UK+biobank+cohort+study.">Relationship among diabetes, obesity, and cardiovascular disease phenotypes: A UK biobank cohort study.</a> Diabetes Care. 46 (8), 1531-1540 (2023).</li></ol>

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
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			<td>GS Biotech</td>
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			<td>BD Venflon Pro Safety 14 g x 45 mm, Orange, 50/pk</td>
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			<td>Miltenyi Biotec</td>
			<td>130-118-495</td>
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			<td>C10337</td>
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			<td>Corning&#160;</td>
			<td>354230</td>
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			<td>3526</td>
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			<td>3516</td>
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			<td>LS Columns, 25/pk</td>
			<td>Miltenyi Biotec</td>
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			<td>Invitrogen</td>
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			<td>130-042-109</td>
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			<td>Miltenyi Biotec</td>
			<td>130-041-407</td>
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			<td>Cell Signalling Technology</td>
			<td>4087</td>
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			<td>Miltenyi Biotec</td>
			<td>130-090-976</td>
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			<td>62.554.502</td>
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			<td>Sarstedt</td>
			<td>62.547.254</td>
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			<td>Screw cap tube, 50 ml, (Lx&#216;): 114 x 28 mm, PP, with print</td>
			<td>Sarstetd</td>
			<td>62.547.254</td>
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			<td>BD Biosciences</td>
			<td>610297</td>
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			<td>Merck</td>
			<td>93443-500ML</td>
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			<td>&#946;-Actin (C4) Mouse 1:5000</td>
			<td>Santa Cruz Biotechnology</td>
			<td>&#160;Sc-47778</td>
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</table>

studying adipose endothelial cell/adipocyte cross-talk in human subcutaneous adipose tissue

Endothelial cells (ECs) are squamous cells that line the inner surface of the blood vessel wall as a monolayer. They have many essential roles, including control of vascular tone, regulation of thrombosis, modulating the inflammatory response, and contributing to angiogenesis1. Given the importance of endothelial cells in cardiometabolic physiology, they are frequently used experimentally to further the understanding of pathophysiology and to examine new pharmacological treatments for cardiometabolic disease.
However, there is enormous heterogeneity in endothelial cell morphology, function, gene expression, and antigen composition depending on the origin of their vascular bed2. While endothelial cells from large arteries are best suited to atherosclerosis studies, endothelial cells from small vessels, known as microvascular endothelial cells (MVECs), are more suitable for angiogenesis studies2. Understanding the molecular basis for endothelial heterogeneity may provide valuable insights into vascular bed-specific therapies. Microvascular endothelial function also significantly differs in numerous diseases, including diabetes, cardiovascular disease, and systemic infection3,4. Therefore, the ability to isolate endothelial cells from defined patient groups allows direct comparison of their endothelial cell function and cellular cross-talk5. 
In this paper, we describe a novel method of isolating human MVECs from subcutaneous adipose tissue (hSATMVEC) taken at the time of cardiac implantable electronic device (CIED) insertion. hSATMVEC isolated following enzymatic digestion of subcutaneous adipose tissue (SAT) were grown and passaged on gelatin-coated plates. We then describe a range of phenotyping assays that have been successfully applied to hSATMVECs in order to validate their phenotype and demonstrate use in routine endothelial cell assays. Finally, we describe an application of hSATMVECs in an experimental model of hSATMVECs-adipocyte cross-talk.

<meta charset="utf8"></head><body>Autore in primo piano: Approfondimenti sulle malattie cardiometaboliche con studi di microvascolarizzazione del tessuto adiposo sottocutaneo

Studio del cross-talk tra cellule endoteliali adipose e adipociti nel tessuto adiposo sottocutaneo umano

Read this Scientific Article Protocol about Studying Adipose Endothelial Cell/Adipocyte Cross-Talk in Human Subcutaneous Adipose Tissue at JoVE.com

Microvascular endothelial cells (MVECs) have many critical roles, including control of vascular tone, regulation of thrombosis, and angiogenesis. ...

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Research

JoVE Journal

Medicine

Studying Adipose Endothelial Cell/Adipocyte Cross-Talk in Human Subcutaneous Adipose Tissue

535 Views.  University of Leeds. Vogliamo capire il ruolo della microvascolarizzazione sottocutanea del tessuto adiposo nelle persone con e senza malattia cardiometabolica. A tal fine, abbiamo isolato cellule endoteliali microvascolari del tessuto adiposo sottocutaneo da pazienti sottoposti a dispositivi elettronici impiantabili cardiaci. Questo serve a studiare il fenotipo delle cellule endoteliali e il crosstalk cellula-cellula con gli adipociti.Storicamente, abbiamo utilizzato line...

Video: Autore in primo piano: Approfondimenti sulle malattie cardiometaboliche con studi di microvascolarizzazione del tessuto adiposo sottocutaneo 

Microvascular endothelial cells (MVECs) have many critical roles, including control of vascular tone, regulation of thrombosis, and angiogenesis. Significant heterogeneity in endothelial cell (EC) genotype and phenotype depends on their vascular bed and host disease state. The ability to isolate MVECs from tissue-specific vascular beds and individual patient groups offers the opportunity to directly compare MVEC function in different disease states. Here, using subcutaneous adipose tissue (SAT) taken at the time of insertion of cardiac implantable electronic devices (CIED), we describe a method for the isolation of a pure population of functional human subcutaneous adipose tissue MVEC (hSATMVEC) and an experimental model of hSATMVEC-adipocyte cross-talk.
hSATMVEC were isolated following enzymatic digestion of SAT by incubation with anti-CD31 antibody-coated magnetic beads and passage through magnetic columns. hSATMVEC were grown and passaged on gelatin-coated plates. Experiments used cells at passages 2-4. Cells maintained classic features of EC morphology until at least passage 5. Flow cytometric assessment showed 99.5% purity of isolated hSATMVEC, defined as CD31+/CD144+/CD45-. Isolated hSATMVEC from controls had a population doubling time of approximately 57 h, and active proliferation was confirmed using a cell proliferation imaging kit. Isolated hSATMVEC function was assessed using their response to insulin stimulation and angiogenic tube-forming potential. We then established an hSATMVEC-subcutaneous adipocyte co-culture model to study cellular cross-talk and demonstrated a downstream effect of hSATMVEC on adipocyte function.
hSATMVEC can be isolated from SAT taken at the time of CIED insertion and are of sufficient purity to both experimentally phenotype and study hSATMVEC-adipocyte cross-talk.

Here, we describe a protocol for isolating, culturing, and phenotyping microvascular endothelial cells from human subcutaneous adipose tissue (hSATMVECs). Additionally, we describe an experimental model of hSATMVEC-adipocyte cross-talk.