Pleiotrophin

Protein in humans From Wikipedia, the free encyclopedia

Pleiotrophin (PTN) also known as heparin-binding brain mitogen (HBBM) or heparin-binding growth factor 8 (HBGF-8) or neurite growth-promoting factor 1 (NEGF1) or heparin affinity regulatory peptide (HARP) or heparin binding growth associated molecule (HB-GAM) is a protein that in humans is encoded by the PTN gene.[5] Pleiotrophin is an 18-kDa growth factor that has a high affinity for heparin. It is structurally related to midkine and retinoic acid induced heparin-binding protein.

AliasesPTN, HARP, HBGF8, HBNF, NEGF1, HB-GAM, HBBM, HBGF-8, HBNF-1, OSF-1, pleiotrophin
External IDsOMIM: 162095; MGI: 97804; GeneCards: PTN
PDBOrtholog search: PDBe RCSB
Quick facts PTN, Identifiers ...
PTN
Identifiers
AliasesPTN, HARP, HBGF8, HBNF, NEGF1, HB-GAM, HBBM, HBGF-8, HBNF-1, OSF-1, pleiotrophin
External IDsOMIM: 162095; MGI: 97804; GeneCards: PTN
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002825
NM_001321386
NM_001321387

NM_008973

RefSeq (protein)

NP_001308315
NP_001308316
NP_002816

NP_032999

Location (UCSC)Chr 7: 137.23 – 137.34 MbChr 6: 36.69 – 36.79 Mb
PubMed search[3][4]
Wikidata
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Function

Pleiotrophin was initially recognized as a neurite outgrowth-promoting factor present in rat brain around birth[6] and as a mitogen toward fibroblasts isolated from bovine uterus tissue.[7] Together with midkine these growth-factors constitute a family of (developmentally regulated) secreted heparin-binding proteins[8] now known as the neurite growth-promoting factor (NEGF) family. During embryonic and early postnatal development, pleiotrophin is expressed in the central and peripheral nervous system and also in several non-neural tissues, notably lung, kidney, gut and bone.[9] Pleiotrophin is also expressed by several tumor cells and is thought to be involved in tumor angiogenesis.[10] In the adult central nervous system, pleiotrophin is expressed in an activity-dependent manner in the hippocampus[11][12] where it can suppress long term potentiation induction.[13] Pleiotrophin expression is low in other areas of the adult brain, but it can be induced by ischemic insults.[14][15] or targeted neuronal damaged in the entorhinal cortex or in the substantia nigra pars compacta.

Clinical significance

Pleiotrophin binds to cell-surface nucleolin as a low affinity receptor. This binding can inhibit HIV infection.[16]

References

Further reading

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