Side population cells isolated from different tissues share transcriptome signatures and express tissue-specific markers

Exp Cell Res. 2005 Feb 15;303(2):360-74. doi: 10.1016/j.yexcr.2004.10.011. Epub 2004 Nov 11.

Abstract

Side Population (SP) cells, isolated from murine adult bone marrow (BM) based on the exclusion of the DNA dye Hoechst 33342, exhibit potent hematopoietic stem cell (HSC) activity when compared to Main Population (MP) cells. Furthermore, SP cells derived from murine skeletal muscle exhibit both hematopoietic and myogenic potential in vivo. The multipotential capacity of SP cells isolated from variable tissues is supported by an increasing number of studies. To investigate whether the SP phenotype is associated with a unique transcriptional profile, we characterized gene expression of SP cells isolated from two biologically distinct tissues, bone marrow and muscle. Comparison of SP cells with differentiated MP cells within a tissue revealed that SP cells are in an active transcriptional and translational status and underexpress genes reflecting tissue-specific functions. Direct comparison of gene expression of SP cells isolated from different tissues identified genes common to SP cells as well as genes specific to SP cells within a particular tissue and further define a muscle and bone marrow environment. This study reports gene expression of muscle SP cells, common features and differences between SP cells isolated from muscle and bone marrow, and further identifies common signaling pathways that might regulate SP cell functions.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bone Marrow Cells / classification
  • Bone Marrow Cells / cytology*
  • Bone Marrow Cells / metabolism*
  • Cell Separation
  • Gene Expression*
  • Genetic Markers
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Fibers, Skeletal / classification
  • Muscle Fibers, Skeletal / cytology
  • Muscle Fibers, Skeletal / metabolism
  • Muscle, Skeletal / cytology*
  • Muscle, Skeletal / metabolism*
  • Organ Specificity
  • Signal Transduction
  • Transcription, Genetic

Substances

  • Genetic Markers