The authors want to thank Dr. Ivo Kalajzic for the &#945;SMA-GFP mice. Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health (NIH) under Award Number R01GM118300 (S.S.), National Institute of Biomedical Imaging and Bioengineering of the NIH under Award Number R21EB019509 (P.P.Y.), and Scientist Development Grant of the American Heart Association under Award Number 17SDG33630187 (S.S.). Flow cytometry analyses were performed at the VUMC Flow Cytometry Shared Resource which is supported by the Vanderbilt Ingram Cancer Center (P30 CA68485) and the Vanderbilt Digestive Disease Research Center (DK058404).

<ol>
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A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=View+from+the+heart:+cardiac+fibroblasts+in+development,+scarring+and+regeneration.">View from the heart: cardiac fibroblasts in development, scarring and regeneration.</a> Development. 143 (3), 387-397 (2016).</li><li>Stellato, M., Czepiel, M., Distler, O., Blyszczuk, P., Kania, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Identification+and+Isolation+of+Cardiac+Fibroblasts+From+the+Adult+Mouse+Heart+Using+Two-Color+Flow+Cytometry.">Identification and Isolation of Cardiac Fibroblasts From the Adult Mouse Heart Using Two-Color Flow Cytometry.</a> Frontiers in Cardiovascular Medicine. 6, 105 (2019).</li><li>Ackers-Johnson, 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=A+Simplified,+Langendorff-Free+Method+for+Concomitant+Isolation+of+Viable+Cardiac+Myocytes+and+Nonmyocytes+From+the+Adult+Mouse+Heart.">A Simplified, Langendorff-Free Method for Concomitant Isolation of Viable Cardiac Myocytes and Nonmyocytes From the Adult Mouse Heart.</a> Circulatory Research. 119 (8), 909-920 (2016).</li><li>Saraswati, S., Marrow, S. 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T., Eghbali, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulation+of+fibrillar+collagen+types+I+and+III+and+basement+membrane+type+IV+collagen+gene+expression+in+pressure+overloaded+rat+myocardium.">Regulation of fibrillar collagen types I and III and basement membrane type IV collagen gene expression in pressure overloaded rat myocardium.</a> Circulatory Research. 67 (4), 787-794 (1990).</li><li>Vasquez, C., Benamer, N., Morley, G. 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R., 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=Revisiting+Cardiac+Cellular+Composition.">Revisiting Cardiac Cellular Composition.</a> Circulatory Research. 118 (3), 400-409 (2016).</li></ol>

The authors have nothing to disclose.

Fibroblasts are a heterogenous group of cells, identified by diverse set of markers. The protein markers that have been used to identify fibroblasts are discoidin domain receptor 2 (DDR2), fibronectin, vimentin, collagen I and III, and Thy115,16,17,18,19,20. Whereas vimentin has been used to identify uninjured quiescent cardi...

Cardiac fibroblasts, cells of mesenchymal origin, play a significant role in maintaining the electrical conduction and mechanical forces in the heart in addition to the maintenance of cardiac architecture during homeostasis1. Following injury, these cells are activated, expand, and produce extracellular matrix (ECM) proteins2. Many preclinical studies have revealed fibroblasts as critical cellular regulators that maintain the structural integrity of an injured heart3 as well as main effector cells responsible for unchecked production and deposition of ECM proteins, resulting in stiff scar formation and heart failure4. Fibroblasts are a heterogenous group of cells, making it challenging to dissect their reparative function from pro-fibrotic maladaptive properties. Recently, the functional heterogeneity of two distinct fibroblast subtypes following myocardial injury have been defined, indicating the possibility of isolating different fibroblast subtypes and studying their role in wound healing5.
Obtaining a pure fibroblast population is crucial in delineating their functional role in repair and fibrosis. However, the presence of multiple fibroblast markers that recognize other cell types make it challenging to isolate a substantially pure fibroblast population6. Several elegant studies have devised clever ways to isolate cardiac fibroblasts from uninjured and injured myocardium. The most popular and well-established method of enriching fibroblasts is through selective adhesion following enzymatic tissue digestion7.
Additionally, fluorescence-activated cell sorting (FACS) of fibroblasts based on cell surface antigens has been successfully described8. In the study, following enzymatic digestion, the mesenchymal cells were sorted as lineage-negative (Lin: Ter119&#8722;CD45&#8722;CD31&#8722;) and gp38-positive (gp38+) from mouse hearts. Gp38+ve cells were confirmed to be fibroblasts based on their co-expression of col1&#945;1 and other mesenchymal markers. Although most tissue digestion is completed after dissecting out the ventricle in a Petri dish, a recent study has investigated the use of a direct needle enzyme perfusion of the left ventricle to isolate myocytes and non-myocytes which include fibroblasts9. Fibroblasts were then isolated by selective adhesion in this case.
This protocol describes the isolation and enrichment of fibroblasts using three methods. The first is an already established method involving selective adhesion of fibroblasts following enzymatic digestion. The second method is used to primarily isolate injury-induced alpha smooth muscle expressing myofibroblasts. The third method involves sequential, magnetic depletion of an enzyme-digested cardiac cell suspension of hematopoietic and endothelial cells. Following depletion, fibroblasts/myofibroblasts are isolated based on the presence of the antigen MEFSK4 using magnetic beads. Recently, MEFSK4 has been described as an antigen present on quiescent as well as activated fibroblasts, making it a suitable marker for fibroblast identification and isolation. Naturally, all the methods described here have unique limitations. It is therefore highly recommended to check the purity of the isolated cell population by flow analysis, immunostaining, and semi-quantitative real-time PCR. However, these methodologies can be expanded upon, and additional markers can be added in order to exclude other contaminating populations prior to utilizing the fibroblast and myofibroblast populations for crucial experiments.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Reagents</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Acetone</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Anti-fungal (Amphotericin B-solubilized; Fungizone)</td>
			<td>Sigma Aldrich</td>
			<td>A9528</td>
			<td></td>
		</tr>
		<tr>
			<td>Bovine Serium Albumin (BSA)</td>
			<td>Sigma</td>
			<td>9048-46-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Calcium chloride</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Citrate Buffer</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Collagenase blend (Liberase Blendzyme 3 TH)</td>
			<td>Roche Applied Science</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>DAPI</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>DDI water</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>DI water</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>DMEM-F12 with L-Glutamine and HEPES</td>
			<td>Life technologies</td>
			<td>11330057</td>
			<td></td>
		</tr>
		<tr>
			<td>Dnase I(20U/mL)</td>
			<td>BioRad</td>
			<td>7326828</td>
			<td></td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s Phosphate-Buffered Saline (dPBS) without Ca2+ and Mg2+</td>
			<td>Gibco</td>
			<td>13190-144</td>
			<td></td>
		</tr>
		<tr>
			<td>70% Ethanol</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FC Blocker (Purified anti-mouse CD16/CD32)</td>
			<td>Tonbo Biosciences</td>
			<td>70-0161</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal Bovine Serum (FBS)</td>
			<td>Life technologies</td>
			<td>16000044</td>
			<td></td>
		</tr>
		<tr>
			<td>10% goat serum</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Hank&#39;s Balanced Salt Solution (HBSS) with Ca2+ and Mg2+</td>
			<td>Corning</td>
			<td>21-023-CV</td>
			<td></td>
		</tr>
		<tr>
			<td>1M HEPES</td>
			<td>Corning</td>
			<td>25-060-Ci</td>
			<td></td>
		</tr>
		<tr>
			<td>Krebs-Henseleit Buffer powder</td>
			<td>Sigma</td>
			<td>K3753</td>
			<td></td>
		</tr>
		<tr>
			<td>Mycoplasma prophylactic (Plasmocin)</td>
			<td>Invivogen</td>
			<td>ant-mpp</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin/Streptomycin</td>
			<td>Thermo Fisher Scientific</td>
			<td>15140122</td>
			<td></td>
		</tr>
		<tr>
			<td>1x Phosphate-Buffered Saline (PBS)</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>10x Red Blood Cell Lysis Buffer</td>
			<td>Miltenyi</td>
			<td>130-094-183</td>
			<td></td>
		</tr>
		<tr>
			<td>Slow-fade Mounting Media</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium azide</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium bicarbonate</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>TGF&#946;</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Trypan Blue Stain (0.4%)</td>
			<td>Gibco</td>
			<td>15250-061</td>
			<td></td>
		</tr>
		<tr>
			<td>Type 1 Rat Collagen</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Antibodies</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>7AAD (stock: 1 mg/mL solution in DMSO)</td>
			<td>Molecular Probes</td>
			<td>A1310</td>
			<td>dilution = 1:1000; RRID =</td>
		</tr>
		<tr>
			<td>CD45-APC</td>
			<td>BD Bioscience</td>
			<td>559864</td>
			<td>dilution = 1:200; RRID = AB_398672</td>
		</tr>
		<tr>
			<td>CD31-PE</td>
			<td>BD Bioscience</td>
			<td>553373</td>
			<td>dilution = 1:200; RRID = AB_394819</td>
		</tr>
		<tr>
			<td>CD31</td>
			<td>BD Biosciences</td>
			<td>553370</td>
			<td>dilution = 1:250; RRID = AB_394816</td>
		</tr>
		<tr>
			<td>CD45</td>
			<td>BD Biosciences</td>
			<td>553076</td>
			<td>dilution = 1:250; RRID = AB_394606</td>
		</tr>
		<tr>
			<td>COL 1&#945;1</td>
			<td>MD Bioproducts</td>
			<td>203002</td>
			<td>dilution = 1:1000; RRID =</td>
		</tr>
		<tr>
			<td>Ghost dye violet 510 (Formulation: 1 uL/test in DMSO)</td>
			<td>Tonbo Biosciences</td>
			<td>13-0870</td>
			<td>dilution = 1:1000; RRID =</td>
		</tr>
		<tr>
			<td>Goat anti-mouse Alexa Fluor 488</td>
			<td>Molecular Probes</td>
			<td>A11029</td>
			<td>dilution = 1:200; RRID = AB_138404</td>
		</tr>
		<tr>
			<td>Goat anti-rabbit-Cy3</td>
			<td>Southern Biotech</td>
			<td>4050-02</td>
			<td>dilution = 1:200; RRID = AB_2795952</td>
		</tr>
		<tr>
			<td>Goat anti-rabbit-FITC</td>
			<td>Jackson Immunoresearch Laboratories</td>
			<td>711-165-152</td>
			<td>dilution = 1:200; RRID = AB_2307443</td>
		</tr>
		<tr>
			<td>Goat anti-rat Alexa Fluor 488</td>
			<td>Molecular Probes</td>
			<td>A11006</td>
			<td>dilution = 1:200; RRID = AB_2534074</td>
		</tr>
		<tr>
			<td>Goat anti-rat Alexa Fluor 647</td>
			<td>Thermo-Fisher</td>
			<td>A21247</td>
			<td>dilution = 1:200; RRID = AB_141778</td>
		</tr>
		<tr>
			<td>Periostin</td>
			<td>Santa Cruz</td>
			<td>SC67233</td>
			<td>dilution = 1:100; RRID = AB_2166650</td>
		</tr>
		<tr>
			<td>Vimentin</td>
			<td>Sigma Aldrich</td>
			<td>V2258</td>
			<td>dilution = 1:200; RRID = AB_261856</td>
		</tr>
		<tr>
			<td>&#945;-smooth muscle actin (&#945;SMA)</td>
			<td>Sigma Aldrich</td>
			<td>A2547</td>
			<td>dilution = 1:1000; RRID = AB_476701</td>
		</tr>
		<tr>
			<td>Fibroblast specific protein 1 (FSP1)</td>
			<td>Millipore 07-2274</td>
			<td>07-2274</td>
			<td>dilution = 1:100; RRID = AB_10807552</td>
		</tr>
		<tr>
			<td>CD45 Magnetic Beads</td>
			<td>Miltenyi Biotec</td>
			<td>130-052-301</td>
			<td></td>
		</tr>
		<tr>
			<td>CD31 Magnetic Beads</td>
			<td>Miltenyi Biotec</td>
			<td>130-087-418</td>
			<td></td>
		</tr>
		<tr>
			<td>Anti-feeder cells-APC (MEFSK4)</td>
			<td>Miltenyi Biotec</td>
			<td>130-102-900</td>
			<td>dilution = 1:100; RRID = AB_2660619</td>
		</tr>
		<tr>
			<td>anti-APC Beads</td>
			<td>Miltenyi Biotec</td>
			<td>130-090-855</td>
			<td></td>
		</tr>
		<tr>
			<td>Rat IgG-APC</td>
			<td>Miltenyi Biotec</td>
			<td>130-103-034</td>
			<td>dilution = 1:100; RRID = AB_2661598</td>
		</tr>
		<tr>
			<td>Donkey anti-rat Alexa Fluor405</td>
			<td>Abcam</td>
			<td>ab175670</td>
			<td>dilution = 1:100</td>
		</tr>
		<tr>
			<td>anti-AN2/NG2</td>
			<td>Miltenyi Biotec</td>
			<td>130-097-455</td>
			<td>dilution = 1:11; RRID = AB_2651235</td>
		</tr>
		<tr>
			<td>Other Materials</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>0.22 &#181;m Filter</td>
			<td>Thermo Scientific</td>
			<td>723-2520</td>
			<td></td>
		</tr>
		<tr>
			<td>10 cm2 Cell Culture Dish</td>
			<td>Corning</td>
			<td>430167</td>
			<td></td>
		</tr>
		<tr>
			<td>10 mL Pipet</td>
			<td>Fisherbrand</td>
			<td>13-678-11E</td>
			<td></td>
		</tr>
		<tr>
			<td>40 &#181;m Cell Strainer</td>
			<td>Fisherbrand</td>
			<td>22363547</td>
			<td></td>
		</tr>
		<tr>
			<td>5 mL Pipet</td>
			<td>Fisherbrand</td>
			<td>13-678-11D</td>
			<td></td>
		</tr>
		<tr>
			<td>50 mL Conical Tube</td>
			<td>Falcon</td>
			<td>352070</td>
			<td></td>
		</tr>
		<tr>
			<td>6-well Plate</td>
			<td>Corning</td>
			<td>3506</td>
			<td></td>
		</tr>
		<tr>
			<td>Flow Cytometry Tubes</td>
			<td>Falcon</td>
			<td>352058</td>
			<td></td>
		</tr>
		<tr>
			<td>Forceps</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Rocker</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Single Edge Blade</td>
			<td>PAL</td>
			<td>62-0177</td>
			<td></td>
		</tr>
		<tr>
			<td>Surgical Scissors</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>GFP-&#945;SMA Reporter Mice</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>MACS Separator Magnetic Field</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>MACS Separation Column</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Coverslips</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Qaigen Rneasy Mini Kit</td>
			<td>Qaigen</td>
			<td>74104</td>
			<td></td>
		</tr>
		<tr>
			<td>Ambion RNAqueous Micro Total Isolation Kit</td>
			<td>Ambion</td>
			<td>AM1931</td>
			<td></td>
		</tr>
		<tr>
			<td>BioRad iScript cDNA Syntehsis Kit</td>
			<td>BioRad</td>
			<td>1708891</td>
			<td></td>
		</tr>
		<tr>
			<td>48-well Plate</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>30G Needle</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>3 Laser Flow Cytometry Machine (BD LSRFortessa)</td>
			<td>BD Biosciences</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>4 Laser Flow Cytometry Machine (BD FACSAria III)</td>
			<td>BD Biosciences</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Flow Data Acquiring Software (BD FACSDiva Software v8.0a)</td>
			<td>BD Biosciences</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Flow Data Analysis Software (FlowJo Software)</td>
			<td>BD Biosciences</td>
			<td></td>
			<td></td>
		</tr>
	</tbody>
</table>

isolation and characterization of adult cardiac fibroblasts and myofibroblasts

Cardiac fibrosis in response to injury is a physiological response to wound healing. Efforts have been made to study and target fibroblast subtypes that mitigate fibrosis. However, fibroblast research has been hindered due to the lack of universally acceptable fibroblast markers to identify quiescent as well as activated fibroblasts. Fibroblasts are a heterogenous cell population, making them difficult to isolate and characterize. The presented protocol describes three different methods to enrich fibroblasts and myofibroblasts from uninjured and injured mouse hearts. Using a standard and reliable protocol to isolate fibroblasts will enable the study of their roles in homeostasis as well as fibrosis modulation.

Flow gating scheme demonstrating myofibroblast isolation using &#945;SMA-GFP reporter mice 
Uninjured hearts showed no detectable GFP+ cells in &#945;SMA-GFP reporter mouse model; hence, they were used to establish a gate for the background signal of the GFP channel post-compensation (Figure 2). &#945;SMA+ cells were sorted based on the presence of GFP expression from the injured left ventricle 10 days following MI. A small percentage of endothelia...

Watch this Scientific Journal Video about Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts at JoVE.com

Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts

Obtaining a pure population of fibroblasts is crucial to studying their role in wound repair and fibrosis. Described here is a detailed method to isolate fibroblasts and myofibroblasts from uninjured and injured mouse hearts followed by characterization of their purity and functionality by immunofluorescence, RTPCR, fluorescence-assisted cell sorting, and collagen gel contraction.

Cardiac fibrosis in response to injury is a physiological response to wound healing. Efforts have been made to study and target fibroblast subtypes that ...

isolation-characterization-adult-cardiac-fibroblasts

Research

JoVE Journal

Biology

15.6K Views.  Vanderbilt University Medical Center. Obtaining a pure population of fibroblasts is crucial to studying their role in wound repair and fibrosis. Described here is a detailed method to isolate fibroblasts and myofibroblasts from uninjured and injured mouse hearts followed by characterization of their purity and functionality by immunofluorescence, RTPCR, fluorescence-assisted cell sorting, and collagen gel contraction.

Video: Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts

Isolation and Genetic Manipulation of Adult Cardiac Myocytes for Confocal Imaging

Cardiac myocytes isolated from adult hearts are widely accepted as a model somewhere half way between embryonic and neonatal muscle cells on one side and a working heart on the other. Thus, cardiomyocytes serve as good models for cardiac cellular physiology and pathophysiology, for pharmaceutical investigations as well as for the exploration of transgenic animal models. Here we describe a method of isolating the cells from the heart. Furthermore we show how a genetic manipulation on cardiac myocytes can be performed without breeding a transgenic animal: This is the combination of long term culture (1 week) and adenoviral gene transfer. The latter one is described from the construction of the virus to the transduction of the cells. It can be used for the expression of genetically encoded biosensors (GEBs), fluorescent fusion proteins, but also for protein over expression and down regulation, e.g. using RNAi. Here we provide an example for the expression of a fusion protein staining a subcellular structure (Golgi). Such protein expression can be visualized by confocal imaging of z-stacks for a 3D-reconstruction of subcellular structures. The protocol comprises state-of-the-art in cell culture, molecular biology and biophysics and thus provides an approach for exploring new horizons in cellular cardiology.

Adult cardiac myocytes are primary cells that can be isolated from animal hearts and cultured for several days. Within this culture period adenoviral gene transfer can be used to express genetically encoded biosensors (GEBs) or fluorescent fusion proteins. Both approaches allow cellular investigations by means of confocal microscopy.

Cardiac myocytes isolated from adult hearts are widely accepted as a model somewhere half way between embryonic and neonatal muscle cells on one side and ...

Isolation, Culture, and Functional Characterization of Adult Mouse Cardiomyoctyes

The use of primary cardiomyocytes (CMs) in culture has provided a powerful complement to murine models of heart disease in advancing our understanding of heart disease. In particular, the ability to study ion homeostasis, ion channel function, cellular excitability and excitation-contraction coupling and their alterations in diseased conditions and by disease-causing mutations have led to significant insights into cardiac diseases. Furthermore, the lack of an adequate immortalized cell line to mimic adult CMs, and the limitations of neonatal CMs (which lack many of the structural and functional biomechanics characteristic of adult CMs) in culture have hampered our understanding of the complex interplay between signaling pathways, ion channels and contractile properties in the adult heart strengthening the importance of studying adult isolated cardiomyocytes. Here, we present methods for the isolation, culture, manipulation of gene expression by adenoviral-expressed proteins, and subsequent functional analysis of cardiomyocytes from the adult mouse. The use of these techniques will help to develop mechanistic insight into signaling pathways that regulate cellular excitability, Ca2+ dynamics and contractility and provide a much more physiologically relevant characterization of cardiovascular disease.

Here we describe the isolation of adult mouse cardiomyoctyes using a Langendorff perfusion system. The resulting cells are Ca2+-tolerant, electrically quiescent and can be cultured and transfected with adeno- or lentiviruses to manipulate gene expression. Their functionality can also be analyzed using the MMSYS system and patch clamp techniques.

The use of primary cardiomyocytes (CMs) in culture has provided a powerful complement to murine models of heart disease in advancing our understanding of ...

Isolation of Primary Myofibroblasts from Mouse and Human Colon Tissue

The myofibroblast is a stromal cell of the gastrointestinal (GI) tract that has been gaining considerable attention for its critical role in many GI functions. While several myofibroblast cell lines are commercially available to study these cells in vitro, research results from a cell line exposed to experimental cell culture conditions have inherent limitations due to the overly reductionist nature of the work. Use of primary myofibroblasts offers a great advantage in terms of confirming experimental findings identified in a cell line. Isolation of primary myofibroblasts from an animal model allows for the study of myofibroblasts under conditions that more closely mimic the disease state being studied. Isolation of primary myofibroblasts from human colon tissue provides arguably the most relevant experimental data, since the cells come directly from patients with the underlying disease. We describe a well-established technique that can be utilized to isolate primary myofibroblasts from both mouse and human colon tissue. These isolated cells have been characterized to be alpha-smooth muscle actin and vimentin-positive, and desmin-negative, consistent with subepithelial intestinal myofibroblasts. Primary myofibroblast cells can be grown in cell culture and used for experimental purposes over a limited number of passages.

The myofibroblast is an influential stromal cell of the gastrointestinal tract that regulates important physiologic processes in both normal and disease states. We describe a technique that allows for the isolation of primary myofibroblasts from both mouse and human colon tissue, which can be utilized for in vitro experimentation.

The myofibroblast is  a stromal cell of the gastrointestinal (GI) tract that has been gaining  considerable attention for its critical role in many GI ...

Isolation and Culture of Adult Mouse Cardiomyocytes for Cell Signaling and in vitro Cardiac Hypertrophy

Technological advances have made genetically modified mice, including transgenic and gene knockout mice, an essential tool in many research fields. Adult cardiomyocytes are widely accepted as a good model for cardiac cellular physiology and pathophysiology, as well as for pharmaceutical intervention. Genetically modified mice preclude the need for complicated cardiomyocyte infection processes to generate the desired genotype, which are inefficient due to cardiomyocytes&#8217; terminal differentiation. Isolation and culture of high quantity and quality functional cardiomyocytes will dramatically benefit cardiovascular research and provide an important tool for cell signaling transduction research and drug development. Here, we describe a well-established method for isolation of adult mouse cardiomyocytes that can be implemented with little training. The mouse heart is excised and cannulated to an isolated heart system, then perfused with a calcium-free and high potassium buffer followed by type II collagenase digestion in Langendorff retrograde perfusion mode. This protocol yields a consistent result for the collection of functional adult mouse cardiomyocytes from a variety of genetically modified mice.

Isolation and Culture of Adult Mouse Cardiomyocytes for Cell Signaling and in vitro Cardiac Hypertrophy

We describe a reliable method for isolation of adult mouse cardiomyocytes. This protocol yields a consistent result for the culture of functional adult cardiomyocytes from a variety of genetically modified mice.

Technological advances have made genetically modified mice, including transgenic and gene knockout mice, an essential tool in many research fields. Adult ...

Isolation of Myofibroblasts from Mouse and Human Esophagus

Murine and human esophageal myofibroblasts are generated via enzymatic digestion. Neonate (8-12 day old) murine esophagus is harvested, minced, washed, and subjected to enzymatic digestion with collagenase and dispase for 25 min. Human esophageal resection specimens are stripped of muscularis propria and adventitia and the remaining mucosa is minced, and subjected to enzymatic digestion with collagenase and dispase for up to 6 hr. Cultured cells express &#945;-SMA and vimentin and express desmin weakly or not at all. Culture conditions are not conducive to growth of epithelial, hematopoietic, or endothelial cells. Culture purity is further confirmed by flow cytometric evaluation of cell surface marker expression of potential contaminating hematopoietic and endothelial cells. The described technique is straightforward and results in consistent generation of non-hematopoieitc, non-endothelial stromal cells. Limitations of this technique are inherent to the use of primary cultures in molecular biology studies, i.e., the unavoidable variability encountered among cultures established across different mice or humans. Primary cultures however are a more representative reflection of the in vivo state compared to cell lines. These methods also provide investigators the ability to isolate and culture stromal cells from different clinical and experimental conditions, allowing comparisons between groups. Characterized esophageal stromal cells can also be used in functional studies investigating epithelial-stromal interactions in esophageal disorders.

We present a protocol to generate primary cultures of murine and human esophageal stromal cells with a myofibroblast phenotype. Cultured cells have spindle shaped morphology, express &#945;-SMA and vimentin, and lack epithelial, hematopoietic and endothelial cell surface markers. Characterized stromal cells can be used in functional studies of epithelial-stromal interactions.

Murine and human esophageal myofibroblasts are generated via enzymatic digestion. Neonate (8-12 day old) murine esophagus is harvested, minced, washed, ...

Methods for the Isolation, Culture, and Functional Characterization of Sinoatrial Node Myocytes from Adult Mice

Sinoatrial node myocytes (SAMs) act as the natural pacemakers of the heart, initiating each heart beat by generating spontaneous action potentials (APs). These pacemaker APs reflect the coordinated activity of numerous membrane currents and intracellular calcium cycling. However the precise mechanisms that drive spontaneous pacemaker activity in SAMs remain elusive. Acutely isolated SAMs are an essential preparation for experiments to dissect the molecular basis of cardiac pacemaking. However, the indistinct anatomy, complex microdissection, and finicky enzymatic digestion conditions have prevented widespread use of acutely isolated SAMs. In addition, methods were not available until recently to permit longer-term culture of SAMs for protein expression studies. Here we provide a step-by-step protocol and video demonstration for the isolation of SAMs from adult mice. A method is also demonstrated for maintaining adult mouse SAMs in vitro and for expression of exogenous proteins via adenoviral infection. Acutely isolated and cultured SAMs prepared via these methods are suitable for a variety of electrophysiological and imaging studies.

Methods are demonstrated for the isolation of sinoatrial node myocytes (SAMs) from adult mice for patch clamp electrophysiology or imaging studies. Isolated cells can be used directly or can be maintained in culture to permit expression of proteins of interest, such as genetically encoded reporters.

Sinoatrial node myocytes (SAMs) act as the natural pacemakers of the heart, initiating each heart beat by generating spontaneous action potentials (APs). ...

Isolation and Characterization of Microvesicles from Peripheral Blood

The release of extracellular vesicles (EVs) including small endosomal-derived exosomes (Exos, diameter &#60; 100 nm) and large plasma membrane-derived microvesicles (MVs, diameter &#62; 100 nm) is a fundamental cellular process that occurs in all living cells. These vesicles transport proteins, lipids and nucleic acids specific for their cell of origin and in vitro studies have highlighted their importance as mediators of intercellular communication. EVs have been successfully isolated from various body fluids and especially EVs in blood have been identified as promising biomarkers for cancer or infectious diseases. In order to allow the study of MV subpopulations in blood, we present a protocol for the standardized isolation and characterization of MVs from peripheral blood samples. MVs are pelleted from EDTA-anticoagulated plasma samples by differential centrifugation and typically possess a diameter of 100 - 600 nm. Due to their larger size, they can easily be studied by flow cytometry, a technique that is routinely used in clinical diagnostics and available in most laboratories. Several examples for quality control assays of the isolated MVs will be given and markers that can be used for the discrimination of different MV subpopulations in blood will be presented.

Extracellular vesicles present in blood have been suggested as novel biomarkers for various diseases. Here, we present a protocol for the isolation of large plasma membrane-derived microvesicles from peripheral blood samples and their subsequent analysis by conventional flow cytometry and Western Blotting.

The release of extracellular vesicles (EVs) including small endosomal-derived exosomes (Exos, diameter &#60; 100 nm) and large plasma membrane-derived ...

Simultaneous Isolation of High Quality Cardiomyocytes, Endothelial Cells, and Fibroblasts from an Adult Rat Heart

The rat is an important animal model used in cardiovascular research, and rat cardiac cells are used routinely for in vitro analysis of the molecular mechanisms of cardiovascular disease progression such as cardiac hypertrophy, fibrosis, and atherosclerosis. Although several attempts with variable success have been made to develop immortalized cell lines from the cardiovascular system to understand these cellular mechanisms, primary cells offer a more natural and close to in vivo environment for such studies. Therefore, different laboratories working on a particular cell type have developed protocols to isolate individual types of rat cardiac cells of interest. A protocol that allows the isolation of more than one cell type, however, is missing. Here an optimized protocol is described that allows the isolation of high-quality major cardiac cell types (cardiomyocytes, endothelial cells, and fibroblasts) from a single preparation and enables their use for cellular analyses. This permits the most efficient use of available resources, which may save time and reduce research costs.

Several protocols have been developed and described for the isolation of different cardiac cell types from a rat heart. Here, an optimized protocol is described that allows the isolation of high-quality major cardiac cell types (cardiomyocytes, endothelial cells, and fibroblasts) from a single preparation, reducing the experimental costs.

The rat is an important animal model used in cardiovascular research, and rat cardiac cells are used routinely for in vitro analysis of the molecular ...

Isolation, Characterization, and Differentiation of Cardiac Stem Cells from the Adult Mouse Heart

Myocardial infarction (MI) is a leading cause of morbidity and mortality around the world. A major goal of regenerative medicine is to replenish the dead myocardium after MI. Although several strategies have been used to regenerate myocardium, stem cell therapy remains a major approach to replenish the dead myocardium of an MI heart. Accumulating evidence suggests the presence of resident cardiac stem cells (CSCs) in the adult heart and their endocrine and/or paracrine effects on cardiac regeneration. However, CSC isolation and their characterization and differentiation toward myocardial cells, especially cardiomyocytes, remains a technical challenge. In the present study, we provided a simple method for the isolation, characterization, and differentiation of CSCs from the adult mouse heart. Here, we describe a density gradient method for the isolation of CSCs, where the heart is digested by a 0.2% collagenase II solution. To characterize the isolated CSCs, we evaluated the expression of CSCs/cardiac markers Sca-1, NKX2-5, and GATA4, and pluripotency/stemness markers OCT4, SOX2, and Nanog. We also determined the proliferation potential of isolated CSCs by culturing them in a Petri dish and assessing the expression of the proliferation marker Ki-67. For evaluating the differentiation potential of CSCs, we selected seven- to ten-days cultured CSCs. We transferred them to a new plate with a cardiomyocyte differentiation medium. They are incubated in a cell culture incubator for 12 days, while the differentiation medium is changed every three days. The differentiated CSCs express cardiomyocyte-specific markers: actinin and troponin I. Thus, CSCs isolated with this protocol have stemness and cardiac markers, and they have a potential for proliferation and differentiation toward cardiomyocyte lineage.

The overall goal of this article is to standardize the protocol for the isolation, characterization, and differentiation of cardiac stem cells (CSCs) from the adult mouse heart. Here, we describe a density gradient centrifugation method to isolate murine CSCs and elaborated methods for CSC culture, proliferation, and differentiation into cardiomyocytes.

Myocardial infarction (MI) is a leading cause of morbidity and mortality around the world. A major goal of regenerative medicine is to replenish the dead ...

Isolation and Characterization of Exosomes from Skeletal Muscle Fibroblasts

Exosomes are small extracellular vesicles released by virtually all cells and secreted in all biological fluids. Many methods have been developed for the isolation of these vesicles, including ultracentrifugation, ultrafiltration, and size exclusion chromatography. However, not all are suitable for large scale exosome purification and characterization. Outlined here is a protocol for establishing cultures of primary fibroblasts isolated from adult mouse skeletal muscles, followed by purification and characterization of exosomes from the culture media of these cells. The method is based on the use of sequential centrifugation steps followed by sucrose density gradients. Purity of the exosomal preparations is then validated by western blot analyses using a battery of canonical markers (i.e., Alix, CD9, and CD81). The protocol describes how to isolate and concentrate bioactive exosomes for electron microscopy, mass spectrometry, and uptake experiments for functional studies. It can easily be scaled up or down and adapted for exosome isolation from different cell types, tissues, and biological fluids.

This protocol illustrates the 1) the isolation and culture of primary fibroblasts from the adult mouse gastrocnemius muscle as well as 2) purification and characterization of exosomes using a differential ultracentrifugation method combined with sucrose density gradients followed by western blot analyses.

Exosomes are small extracellular vesicles released by virtually all cells and secreted in all biological fluids. Many methods have been developed for the ...

Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts

Summary

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Chapters in this video

Isolation and Genetic Manipulation of Adult Cardiac Myocytes for Confocal Imaging

Isolation, Culture, and Functional Characterization of Adult Mouse Cardiomyoctyes

Isolation of Primary Myofibroblasts from Mouse and Human Colon Tissue

Isolation and Culture of Adult Mouse Cardiomyocytes for Cell Signaling and in vitro Cardiac Hypertrophy

Isolation of Myofibroblasts from Mouse and Human Esophagus

Methods for the Isolation, Culture, and Functional Characterization of Sinoatrial Node Myocytes from Adult Mice

Isolation and Characterization of Microvesicles from Peripheral Blood

Simultaneous Isolation of High Quality Cardiomyocytes, Endothelial Cells, and Fibroblasts from an Adult Rat Heart

Isolation, Characterization, and Differentiation of Cardiac Stem Cells from the Adult Mouse Heart

Isolation and Characterization of Exosomes from Skeletal Muscle Fibroblasts