Bone marrow–derived CD8α+TCR− cells that facilitate allogeneic bone marrow transplantation are a mixed population of lymphoid and myeloid progenitors

Gangopadhyay, Nupur N.; Hoffman, Rosemary A.; Shen, Hongmei; Luketich, James D.; Schuchert, Matthew J.

doi:10.1016/j.exphem.2007.07.016

« Previous Next »Experimental Hematology
Volume 35, Issue 12 , Pages 1847-1857, December 2007

Bone marrow–derived CD8α⁺TCR⁻ cells that facilitate allogeneic bone marrow transplantation are a mixed population of lymphoid and myeloid progenitors

Nupur N. Gangopadhyay
- Heart, Lung and Esophageal Surgery Institute, University of Pittsburgh, Pittsburgh, Pa., USA
- Offprint requests to: Nupur N. Gangopadhyay, Ph.D., University of Pittsburgh, University of Pittsburgh Cancer Institute, HCC 2.18B, Research Pavilion, 5117 Centre Avenue, Pittsburgh, PA 15213
Rosemary A. Hoffman
- Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, Pa., USA
Hongmei Shen
- Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, Pa., USA
James D. Luketich
- Heart, Lung and Esophageal Surgery Institute, University of Pittsburgh, Pittsburgh, Pa., USA
Matthew J. Schuchert
- Heart, Lung and Esophageal Surgery Institute, University of Pittsburgh, Pittsburgh, Pa., USA

Received 23 May 2007; received in revised form 12 July 2007; accepted 16 July 2007. published online 08 October 2007.

Objective

We have characterized a hematopoietic cell population isolated from murine bone marrow that can facilitate purified hematopoietic stem cell engraftment across fully allogeneic major histocompatibility complex barriers. These facilitating cells (FCs) are classically identified as CD8α⁺TCR⁻ by flow cytometry. Prior work has demonstrated that FCs are comprised of a heterogeneous cell population with both lymphoid and myeloid phenotypes. The present investigation was designed to more precisely characterize these subsets in terms of both phenotype and developmental potential.

Methods

Using fluorescence-activated cell sorting analysis, freshly isolated FCs were characterized for phenotypic expression of various lymphocyte progenitor markers. The lymphopoietic potential of FCs was evaluated by culturing freshly isolated FCs on bone marrow stroma cells overexpressing notch ligand 1 (OP9-DL1). Transcripts specific to pTα and TCRα were quantitated by employing real-time reverse transcription polymerase chain reaction. Maturation of the T-cell receptor (TCR) on FCs was biochemically analyzed by immunoprecipitation.

Result

Freshly isolated FCs had significant expression of CD44⁺CD25⁻ and CD44⁺CD25⁺ phenotypes. A discrete subset of CD8⁺CD4⁺ cells are also identified in the FC population, similar to the double-positive phase of thymocyte development. Of particular interest, FCs express pre-TCRα (pTα) mRNA and protein as demonstrated by reverse transcription polymerase chain reaction, intracellular staining and immunoprecipitation. FCs grown on OP9-DL1 with interleukin-7 and FMS-like tyrosine kinase 3 ligand can mature into CD44⁻CD25⁺, CD8⁺CD4⁺ and CD8⁺ T cells. During this developmental process, expression of the 33-kDa pTα chain was replaced by a mature 40-kDa TCRα chain.

Conclusion

Taken together, these data demonstrate for the first time that the marrow-derived FC contains a T-cell progenitor population that closely resembles developing thymocytes.