General Information:
Id: | 1,893 |
Diseases: |
Alzheimer disease
- [OMIM]
|
Mammalia | |
review | |
Reference: | Vance JE and Hayashi H(2010) Formation and function of apolipoprotein E-containing lipoproteins in the nervous system Biochim. Biophys. Acta 1801: 806-818 [PMID: 20170744] |
Interaction Information:
Comment | Apo E has also been implicated in the deposition of amyloid plaques since apo E3, more readily than apo E4, forms a complex with Abeta peptides, and mediates the degradation of amyloid deposits. |
Formal Description Interaction-ID: 14493 |
|
Comment | Individuals with one APOE4 isoform are 3 to 4 times as likely to develop AD as those without any APOE4, and people with two APOE4 alleles have a 12-fold higher risk of developing AD. |
Formal Description Interaction-ID: 14500 |
|
Comment | Carriers of the APOE2 allele have decreased risk of developing AD. |
Formal Description Interaction-ID: 14501 |
|
Comment | The APOE4 allele is also associated with an accelerated development and progression of several other neurodegenerative conditions such as Parkinson's disease, multiple sclerosis, head trauma, cerebral hemorrhage and possibly stroke. |
Formal Description Interaction-ID: 14502 |
|
Comment | The APOE isoform E4 allele is also associated with an accelerated development and progression of several other neurodegenerative conditions such as Parkinson's disease, multiple sclerosis, head trauma, cerebral hemorrhage and possibly stroke. |
Formal Description Interaction-ID: 14513 |
|
Comment | The APOE4 allele is also associated with an accelerated development and progression of several other neurodegenerative conditions such as Parkinson's disease, multiple sclerosis, head trauma, cerebral hemorrhage and possibly stroke. |
Formal Description Interaction-ID: 14514 |
|
Comment | The expression of human APOE4, rather than human APOE3, in mice impaired synaptogenesis. |
Formal Description Interaction-ID: 14519 |
|
Comment | Memory and learning were impaired in apo E4 knock-in mice compared to apo E3 knock-in mice. |
Formal Description Interaction-ID: 14521 |
gene/protein mutant decreases_activity of process |
Comment | Mice that express human apo E4 develop 2.5-fold more amyloid deposits than do mice that express human apo E3. |
Formal Description Interaction-ID: 14529 |
|
Comment | ApoJ/ CLU is another apolipoprotein that is abundant in the CNS and has been linked to AD. |
Formal Description Interaction-ID: 14548 |
|
Comment | ApoJ/ CLU has been reported to be a carrier of Abeta across the blood-brain barrier and to suppress Abeta deposition in the brain. |
Formal Description Interaction-ID: 14549 |
|
Comment | The principal cells that secrete apoE in the CNS are astrocytes; microglia also secrete small amounts of apoE. |
Formal Description Interaction-ID: 14550 |
|
Drugbank entries | Show/Hide entries for APOE |
Comment | The principal cells that secrete apoE in the CNS are astrocytes; microglia also secrete small amounts of apoE. |
Formal Description Interaction-ID: 14552 |
|
Drugbank entries | Show/Hide entries for APOE |
Comment | In fibroblasts, human apo E3-containing HDLs from plasma form a complex with ABCA1, and lipid-free apo E inhibits formation of this complex. |
Formal Description Interaction-ID: 14555 |
gene/protein mutant interacts (colocalizes) with complex/PPI HDL |
Comment | In fibroblasts, human apoE3-containing HDLs from plasma form a complex with ABCA1, and lipid-free apoE inhibits formation of this complex. The apo E-ABCA1 interaction does not appear to depend on the isoform of apo E since apo E2, apo E3 and apo E4 bind to ABCA1 with similar affinity. |
Formal Description Interaction-ID: 14557 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | In fibroblasts, human apoE3-containing HDLs from plasma form a complex with ABCA1, and lipid-free apo E inhibits formation of this complex. The apo E-ABCA1 interaction does not appear to depend on the isoform of apo E since apo E2, apo E3 and apo E4 bind to ABCA1 with similar affinity. |
Formal Description Interaction-ID: 14558 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | In fibroblasts, human apoE3-containing HDLs from plasma form a complex with ABCA1, and lipid-free apoE inhibits formation of this complex. The apo E-ABCA1 interaction does not appear to depend on the isoform of apo E since apo E2, apo E3 and apo E4 bind to ABCA1 with similar affinity. |
Formal Description Interaction-ID: 14559 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | The importance of ABCA1 for the lipidation of apo E in the brain is underscored by experiments performed in ABCA1 knock-out mice. |
Formal Description Interaction-ID: 14563 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | ABCG4, are highly expressed in astrocytes and neurons. |
Formal Description Interaction-ID: 14565 |
|
Comment | ABCG4, are highly expressed in astrocytes and neurons. |
Formal Description Interaction-ID: 14567 |
|
Comment | ABCG4 is also highly expressed in microglia, particularly in AD brains. |
Formal Description Interaction-ID: 14568 |
|
Comment | ABCG4 is highly expressed in microglia, particularly in AD brains. |
Formal Description Interaction-ID: 14573 |
|
Comment | The importance of ABCA1 for the lipidation of apo E in the brain is underscored by experiments performed in ABCA1 knock-out mice. |
Formal Description Interaction-ID: 14575 |
|
Drugbank entries | Show/Hide entries for APOE |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 14578 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 14579 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 14580 |
|
Drugbank entries | Show/Hide entries for ABCG1 |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 14581 |
|
Drugbank entries | Show/Hide entries for ABCG1 |
Comment | Apo E has been co-localized with amyloid deposits in plaques and also in neurofibrillary tangles in the brains of AD patients. |
Formal Description Interaction-ID: 14585 |
|
Drugbank entries | Show/Hide entries for APOE |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 46752 |
|
Drugbank entries | Show/Hide entries for ABCA1 |
Comment | The expression of ABCA1 and ABCG1 in macrophages and fibroblasts is markedly increased by activation of the transcription factor LXR (liver X receptor). |
Formal Description Interaction-ID: 46754 |
|
Drugbank entries | Show/Hide entries for ABCG1 |
Comment | The importance of ABCA1 for the lipidation of apo E in the brain is underscored by experiments performed in ABCA1 knock-out mice. |
Formal Description Interaction-ID: 129151 |
|
Drugbank entries | Show/Hide entries for APOE |