The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Molecular cloning of CD68, a human macrophage marker related to lysosomal glycoproteins
Abstract
CD68 is a 110-Kd transmembrane glycoprotein of unknown function highly expressed by human monocytes and tissue macrophages. We have isolated cDNA clones encoding CD68 from a U937 cDNA library by transient expression in COS cells and panning with the anti-CD68 monoclonal antibodies (MoAbs) Y2/131, Y1/82A, EBM11, and Ki-M6. CD68 transcripts are constitutively present in the promonocyte cell line U937 and are upregulated by phorbol myristic acid (PMA). By contrast, CD68 transcripts are absent or present at very low levels in many hematopoietic lines including KG1, CEM, and K562, but can be induced by exposure to PMA. The cDNA sequence predicts a type I integral membrane protein of 354 residues with a heavily glycosylated extracellular domain of 298 residues containing nine potential N-linked glycosylation sites and numerous potential O-linked glycosylation sites. The extracellular domain consists of two distinct regions separated by an extended proline hinge: a membrane-distal mucin-like domain containing short peptide repeats and consisting of 54% serine and threonine residues; and a membrane proximal domain that has significant sequence homology to a family of lysosomal/plasma membrane shuttling proteins known as the lamp 1 group. CD68 is a member of a growing family of hematopoietic mucin-like molecules, including leukosialin/CD43, the stem cell antigen CD34, and the lymph node high endothelial ligand for L-selectin GlyCAM-1.
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DNA sequencing with chain-terminating inhibitors
Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572
A comprehensive set of sequence analysis programs for the VAX
Devereux, J., Haeberli, P., & Smithies, O. (1984) · Nucleic Acids Research · doi:10.1093/nar/12.1part1.387 · Cited by 14,222
Lawrence, M. B., & Springer, T. A. (1991) · Cell · doi:10.1016/0092-8674(91)90393-d · Cited by 2,129
Rapid similarity searches of nucleic acid and protein data banks.
Wilbur, W. J., & Lipman, D. J. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.3.726 · Cited by 1,546
Molecular cloning of a CD28 cDNA by a high-efficiency COS cell expression system.
Aruffo, A., & Seed, B. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.23.8573 · Cited by 784
An endothelial ligand for L-Selectin is a novel mucin-like molecule
Lasky, L. A., Singer, M. S., Dowbenko, D., Imai, Y., Henzel, W. J., Grimley, C., Fennie, C., Gillett, N., Watson, S. R., & Rosent, S. D. (1992) · Cell · doi:10.1016/0092-8674(92)90612-g · Cited by 643
Lysosomal membrane glycoproteins. Structure, biosynthesis, and intracellular trafficking.
Fukuda, M. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54636-6 · Cited by 561
Identification of a specific glycoprotein ligand for P-selectin (CD62) on myeloid cells.
Moore, K. L., Stults, N. L., Diaz, S., Smith, D. F., Cummings, R. D., Varki, A., & McEver, R. P. (1992) · The Journal of cell biology · doi:10.1083/jcb.118.2.445 · Cited by 514
Gordon, S. (1986) · Journal of Cell Science · doi:10.1242/jcs.1986.supplement_4.16 · Cited by 412
Saitoh, O., Wang, W. C., Lotan, R., & Fukuda, M. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42823-2 · Cited by 308
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Metadata
- Authors
- Holness, C., & Simmons, D.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 1993-03-15
- Volume
- 81
- Issue
- 6
- Pages
- 1607-1613
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1539625195
- Cited by
- 733
- References
- 28
- FWCI
- 2.75
- Type
- journal article
- Language
- en
- Open access
- closed
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