A subscription to JoVE is required to view this content. Sign in or start your free trial.

Method Article

A Western Blotting Protocol for Small Numbers of Hematopoietic Stem Cells

10.5K views

⸱

DOI:

10.3791/56855

⸱

August 22nd, 2018

 ,  , 

In This Article

Summary

A standard Western blotting protocol was optimized for analyzing as few as 500 hematopoietic stem or progenitor cells. Optimization involves careful handling of the cell sample, limiting transfers between tubes, and directly lysing the cells in Laemmli sample buffer.

Abstract

Hematopoietic stem cells (HSCs) are rare cells, with the mouse bone marrow containing only ~25,000 phenotypic long term repopulating HSCs. A Western blotting protocol was optimized and suitable for the analysis of small numbers of HSCs (500 - 15,000 cells). Phenotypic HSCs were purified, accurately counted, and directly lysed in Laemmli sample buffer. Lysates containing equal numbers of cells were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and the blot was prepared and processed following standard Western blotting protocols. Using this protocol, 2,000 - 5,000 HSCs can be routinely analyzed, and in some cases data can be obtained from as few as 500 cells, compared to the 20,000 to 40,000 cells reported in most publications. This protocol should be generally applicable to other hematopoietic cells, and enables the routine analysis of small numbers of cells using standard laboratory procedures.

Introduction

Hematopoietic stem cells (HSCs) are self-renewing cells that can give rise to all blood lineages. They are relatively rare cells in the bone marrow, rendering biochemical analyses difficult. Approaches suitable for analyzing rare cells, such as flow cytometry, have been extremely useful for quantifying relative amounts of cell surface markers and intracellular proteins. However, the analysis of intracellular proteins necessitates the use of cell permeabilization procedures to enable antibody access, and not all cell surface epitopes survive these procedures1,2. In addition, antibodies that discriminate between....

Access restricted. Please log in or start a trial to view this content.

Protocol

All procedures must be performed in accordance with institutional animal use and care guidelines. The procedure was developed for the analysis of murine hematopoietic stem and progenitor cells (HSCs and HPs), but can be adapted for the analysis of other cell populations.

1. Flow Cytometry Isolation of Murine HSCs and HPs

  1. Harvest murine bone marrow cells as described in the literature6.
    NOTE: In data presented in Figure 1 and Figure 2, bone marrow was harvested from C57BL/6J mice.
  2. Perform lineage depletion of bone marrow cells usi....

Access restricted. Please log in or start a trial to view this content.

Results

Representative results from 500 - 2,000 purified HSCs and HPs are shown in Figure 1 and Figure 2. The β-actin signal in Figure 1 can be detected from as few as 500 HSCs and HPs purified from the bone marrow of one mouse. Note that loading the lysates into 1.5 mm wells produced a much stronger signal from 500 HPs than loading into 3.0 mm wells. Figure 2 is a Western blot .......

Access restricted. Please log in or start a trial to view this content.

Discussion

Western Blotting is a common technique for detecting specific proteins and the activation of signaling pathways in tissues or cells. By introducing small adjustments to a commonly used procedure, we were able to routinely detect 15 different proteins (Table of Materials) in 15,000 HSCs, and in some cases in as few as 500 HSCs. The most critical steps in this protocol are: 1) accurately counting the cells, 2) minimizing the number of transfers between tubes, and 3) lysing the cells directly with Laemmli s.......

Access restricted. Please log in or start a trial to view this content.

Disclosures

The authors have no conflict of interests to declare.

Acknowledgements

National Institutes of Health grant R01 CA149976 (N.A.S) supported this work.

....

Access restricted. Please log in or start a trial to view this content.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
sodium dodecyl sulfate (SDS)Fisher ScientificBP166-500SDS-PAGE
TEMEDFisher ScientificBP150-20SDS-PAGE
30% Acrylamidel Bis solutionBio-Rad1610158SDS-PAGE
1.5M Tris-HCl pH8.8TEKNOVAT1588SDS-PAGE
1.0M Tris-HCl pH6.8TEKNOVAT1068SDS-PAGE
Ammonium PersulfateFisher ScientificBP179-25SDS-PAGE
mini-protean 3 combBio-Rad1653360SDS-PAGE
Mini-PROTEAN Tetra CellBio-Rad1658005EDUSDS-PAGE
Transfer SystemBio-Rad1704155EDUtransfer
PowerPac HC Power SupplyBio-Rad1645052EDUelectrophoresis
Imaging SystemBio-Rad1708195signal detection
4x Laemmli Sample BufferBio-Rad1610747EDUsample preparation
10x Tris/Glycine/SDS Electrophoresis BufferBio-Rad1610732EDUelectrophoresis
2-MercaptoethanolBio-Rad1610710EDUsample preparation
RTA Mini PVDF Transfer Kit, for 40 blotsBio-Rad1704272transfer
Protease Inhibitor CocktailSigma11697498001sample preparation
Phosphatase Inhibitor CocktailrsGold BiotechnologyGB-450-1sample preparation
EIF4GCell signaling2469WB antibody, validated in 1000 cells
antibody concentration: 1:1000
reference(figure): Fig2
p-Rps6Cell signaling4858WB antibody,validated in 1000 cells
antibody concentration: 1:1000
reference(figure): Fig2
actin(HRP conjugated)abcamab49900WB antibody,validated in 500 cells
antibody concentration: 1:5000
reference(figure): Fig1, Fig2
LC-3Abcamab48394WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig5)
S6Cell Signaling2317WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig4)
4EBP1Cell Signaling9644WB antibody, validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig4)
p-4EBP1Cell Signaling2855WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig4)
TSC2Cell Signaling4308WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig4)
HSP90Cell Signaling4877WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (Fig5)
PTENCell Signaling9188WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (FigS1)
mTORCell Signaling2983WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (FigS1)
p-mTORCell Signaling5536WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (FigS1)
PP2ABCell Signaling4953WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (FigS1)
p-AMPKaCell Signaling2535WB antibody,validated in 15000 cells
antibody concentration: 1:1000
reference(figure): ref5 (FigS1)
actinSanta Cruzsc-47778WB antibody,validated in 15000 cells
antibody concentration: 1:3000
reference(figure): ref5 (Fig4)
lineage depletion kit (mouse)Miltenyi Biotec130-090-858hematopoietic stem and progenitor cells purification
LS columnsMiltenyi Biotec130-041-305hematopoietic stem and progenitor cells purification
SCFPeproTech250-03phosphorylation stimulation
APC-Cy7 c-kit antibodyThermoFisherA15423cell sorting
anti-B220ThermoFisher48-0452-82cell sorting
anti-CD3eThermoFisher48-0031-82cell sorting
anti-Mac1ThermoFisher48-0112-82cell sorting
anti-Gr1ThermoFisher48-5931-82cell sorting
anti-Ter119ThermoFisher48-5921-82cell sorting
Spacer Plates with 1.0 mm Integrated SpacersBio-Rad1653311SDS-PAGE
BSAResearch Products InternationalA30075membrane blocking
serumAtlanta BiologicalsA12450medium supplement
cell counterInvitrogenAMQAF1000cell counting
hemocytometerThermoFisher S17040cell counting
flimDenville ScientificE3012signal detection
medical film processorKonicaSRC-101Asignal detection
Supersignal West Femto Maximum Sensitivity SubstrateTherom Scientific34096signal detection
Allegra X-15R Centrifuge (Rotor SX4750A)Beckman CoulterX-15Rsample preparation
BLUEstain protein ladderGold BiotechnologyP007-500electrophoresis
cell sorterBDFACSAria IIsample preparation
IncublockDenville ScientificI0510electrophoresis

References

  1. Krutzik, P. O., Clutter, M. R., Nolan, G. P. Coordinate analysis of murine immune cell surface markers and intracellular phosphoproteins by flow cytometry. J Immunol. 175 (4), 2357-2365 (2005).
  2. Du, J., et al.

Access restricted. Please log in or start a trial to view this content.

Reprints and Permissions

Explore More Articles

SDS-PAGECell CountingLaemmli Sample BufferPhosphatase InhibitorProteasome InhibitorEnhanced ChemiluminescenceBeta ActinFlow Cytometry