H
Haishan Lin
Publications - 27
Citations - 1698
Haishan Lin is an academic researcher. The author has contributed to research in topics: Receptor & Macrophage colony-stimulating factor. The author has an hindex of 8, co-authored 26 publications receiving 1520 citations.
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Journal ArticleDOI
Discovery of a Cytokine and Its Receptor by Functional Screening of the Extracellular Proteome
Haishan Lin,Ernestine Lee,Kevin Hestir,Cindy Leo,Minmei Huang,Elizabeth Bosch,Robert Halenbeck,Ge Wu,Aileen Zhou,Dirk Behrens,Diane Hollenbaugh,Thomas Linnemann,Minmin Qin,Justin J.-L. Wong,Keting Chu,Stephen K. Doberstein,Lewis T. Williams +16 more
TL;DR: A comprehensive set of recombinant secreted proteins and the extracellular domains of transmembrane proteins, which constitute most of the protein components of the Extracellular space, are produced, useful for discovering new ligands and receptors and assessing the functional selectivity ofextracellular regulatory proteins.
Journal ArticleDOI
Functional overlap but differential expression of CSF-1 and IL-34 in their CSF-1 receptor-mediated regulation of myeloid cells
Suwen Wei,Sayan Nandi,Violeta Chitu,Yee Guide Yeung,Wenfeng Yu,Minmei Huang,Lewis T. Williams,Haishan Lin,E. Richard Stanley +8 more
TL;DR: In this article, the action and expression of IL-34, a novel CSF-1R ligand, were investigated in the mouse, and it was shown that IL34 mRNA was strongly expressed in the embryonic brain at E11.5, prior to the expression of Csf1 mRNA.
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The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation
Sayan Nandi,Solen Gokhan,Xuming Dai,Suwen Wei,Grigori Enikolopov,Haishan Lin,Mark F. Mehler,E. Richard Stanley +7 more
TL;DR: Compared to wild type mice, CSF-1R-deficient mice have smaller brains of greater mass and ablation of the Csf1r gene in Nestin-positive neural progenitors led to a smaller brain size, an expanded Neural progenitor pool and elevated cellular apoptosis in cortical forebrain, indicating novel roles for the CSF/IL-34 receptor in the regulation of corticogenesis.
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Receptor-type Protein-tyrosine Phosphatase ζ Is a Functional Receptor for Interleukin-34
Sayan Nandi,Mario Cioce,Yee Guide Yeung,Edward Nieves,Lydia Tesfa,Haishan Lin,Amy W. Hsu,Robert Halenbeck,Hui Yong Cheng,Solen Gokhan,Mark F. Mehler,E. Richard Stanley +11 more
TL;DR: This study identified receptor-type protein-tyrosine phosphatase ζ (PTP-ζ), a cell surface chondroitin sulfate (CS) proteoglycan, as a novel IL-34 receptor that may mediate its action on novel cellular targets.
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The mechanism of shared but distinct CSF-1R signaling by the non-homologous cytokines IL-34 and CSF-1.
TL;DR: Functional dissection of theIL-34:CSF-1R interface indicates that the hydrophobic interactions, rather than the salt bridge network, dominate the biological activity of IL-34, and to degenerately recognize two ligands with completely different surfaces, CSF- 1R apparently takes advantage of different subsets of a chemically inert surface that can be tuned to fit different ligand shapes.