| Literature DB >> 8980254 |
Y Shimizu1, H Sugiyama, Y Fujii, K Sasaki, K Inoue, H Ogawa, H Tamaki, S Miyake, Y Oji, T Soma, T Yamagami, M Hirata, K Ikeda, T Monden, T Kishimoto.
Abstract
CD45, a transmembrane tyrosine phosphatase, is found on almost all nucleated hematopoietic cells and plays a crucial role in lymphocyte activation and differentiation. We recently achieved isolation of the human LSM-1 (hLSM-1) gene, whose product is a possible substrate for CD45, and we raised antibodies against the hLSM-1 protein. hLSM-1 expression in hematopoietic cells was examined with Northern and Western blot, fluorescence-activated cell sorter, and immunocytochemical analyses. It was found that in the lymphoid lineage, T and B lymphocytes as well as NK cells expressed LSM-1, whereas terminally differentiated plasma cells did not. As for the myeloid lineage, immature myeloid cells expressed LSM-1, whereas terminally differentiated granulocytes and monocytes did not. In the erythroid lineage, normal erythroblasts expressed very low levels of LSM-1, while erythroid cell lines (K562 and HEL) did not. Megakaryocytes did not express LSM-1. Both CD34+/CD33- and CD34+/CD33+ hematopoietic progenitor cells weakly expressed LSM-1. These results showed that LSM-1 is expressed in a lineage- and differentiation stage-specific fashion.Entities:
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Year: 1997 PMID: 8980254 DOI: 10.1002/(sici)1096-8652(199701)54:1<1::aid-ajh1>3.0.co;2-1
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047