العوامل التي يحفزها نقص الأكسجين

(تم التحويل من HIF-1)
العامل 1 الذي يحفزه نقص الأكسجين، الوحدة الجزئية ألفا
hypoxia-inducible factor 1, alpha subunit
المعرفات
الرمزHIF1A
NCBI gene3091
HGNC4910
OMIM603348
RefSeqNM_001530
UniProtQ16665
بيانات أخرى
LocusChr. 14 q21-q24
ابحث عن
البنَىSwiss-model
النطاقاتInterPro
aryl hydrocarbon receptor nuclear translocator
المعرفات
الرمزARNT
الرموز البديلةHIF1B, bHLHe2
NCBI gene405
HGNC700
OMIM126110
RefSeqNM_001668
UniProtP27540
بيانات أخرى
LocusChr. 1 q21
ابحث عن
البنَىSwiss-model
النطاقاتInterPro
endothelial PAS domain protein 1
المعرفات
الرمزEPAS1
الرموز البديلةHIF2A, MOP2, PASD2, HLF
NCBI gene2034
HGNC3374
OMIM603349
RefSeqNM_001430
UniProtQ99814
بيانات أخرى
LocusChr. 2 p21-p16
ابحث عن
البنَىSwiss-model
النطاقاتInterPro
aryl-hydrocarbon receptor nuclear translocator 2
المعرفات
الرمزARNT2
الرموز البديلةHIF2B, KIAA0307, bHLHe1
NCBI gene9915
HGNC16876
OMIM606036
RefSeqNM_014862
UniProtQ9HBZ2
بيانات أخرى
LocusChr. 1 q24
ابحث عن
البنَىSwiss-model
النطاقاتInterPro
العامل 3 الذي يحفزه نقص الأكسجين، الوحدة الجزئية ألفا
hypoxia-inducible factor 3, alpha subunit
المعرفات
الرمزHIF3A
NCBI gene64344
HGNC15825
OMIM609976
RefSeqNM_152794
UniProtQ9Y2N7
بيانات أخرى
LocusChr. 19 q13
ابحث عن
البنَىSwiss-model
النطاقاتInterPro

العوامل التي يحفزها نقص الأكسجين (Hypoxia-inducible factors واختصارها HIFs) هي عوامل النسخ التي تستجيب للانخفاضات في الأكسجين المتاح في البيئة الخلوية، أو نقص الأكسجين.[1][2]

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الاكتشاف

المجمع النسخي للعوامل التي يحفزها نقص الأكسجين اكتشفه في 1995 گرِگ سمنزا وزميله باحث ما بعد الدكتوراه گوانگ وانگ.[3][4][5] في 2016، حصل وليام كيلن، الابن وپيتر راتكليف و گرِگ سمنزا على جائزة لاسكر لعملهم في توضيح دور HIF-1 في الشعور بالأكسجين ودوره في النجاة من الأحوال منخفضة الأكسجين.[6] وفي 2019، حصل الثلاث علماء نفسهم على جائزة نوبل في الفسيولوجيا أو الطب لعملهم في تبيان كيف يشعر HIF ويتكيف للردود الخلوية على توفر الأكسجين.[7]


البنية

Most, if not all, oxygen-breathing species express the highly conserved transcriptional complex HIF-1, which is a heterodimer composed of an alpha and a beta subunit, the latter being a constitutively-expressed aryl hydrocarbon receptor nuclear translocator (ARNT).[8][9] HIF-1 belongs to the PER-ARNT-SIM (PAS) subfamily of the basic helix-loop-helix (bHLH) family of transcription factors. The alpha and beta subunit are similar in structure and both contain the following domains:[10][11][12]

Hypoxia-inducible factor-1
PDB 1lm8 EBI.jpg
Structure of a HIF-1a-pVHL-ElonginB-ElonginC Complex.[13]
المعرفات
الرمزHIF-1
PfamPF11413
HIF-1 alpha C terminal transactivation domain
PDB 1l3e EBI.jpg
Structure of hypoxia-inducible factor-1 alpha subunit.[14]
المعرفات
الرمزHIF-1a_CTAD
PfamPF08778
InterProIPR014887
SCOP1l3e
SUPERFAMILY1l3e

الأعضاء

The following are members of the human HIF family:

العضو الجين الپروتين
HIF-1α HIF1A hypoxia-inducible factor 1, alpha subunit
HIF-1β ARNT aryl hydrocarbon receptor nuclear translocator
HIF-2α EPAS1 endothelial PAS domain protein 1
HIF-2β ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
HIF-3α HIF3A hypoxia inducible factor 3, alpha subunit
HIF-3β ARNT3 aryl-hydrocarbon receptor nuclear translocator 3

الوظيفة

HIF1α expression in Haematopoietic Stem Cells explains the quiescence nature of stem cells[15] for being metabolically maintaining at a low rate so as to preserve the potency of stem cells for long periods in a life cycle of an organism.

The HIF signaling cascade mediates the effects of hypoxia, the state of low oxygen concentration, on the cell. Hypoxia often keeps cells from differentiating. However, hypoxia promotes the formation of blood vessels, and is important for the formation of a vascular system in embryos and tumors. The hypoxia in wounds also promotes the migration of keratinocytes and the restoration of the epithelium.[16]

In general, HIFs are vital to development. In mammals, deletion of the HIF-1 genes results in perinatal death. HIF-1 has been shown to be vital to chondrocyte survival, allowing the cells to adapt to low-oxygen conditions within the growth plates of bones. HIF plays a central role in the regulation of human metabolism.[17]

الآلية

The alpha subunits of HIF are hydroxylated at conserved proline residues by HIF prolyl-hydroxylases, allowing their recognition and ubiquitination by the VHL E3 ubiquitin ligase, which labels them for rapid degradation by the proteasome.[18][19] This occurs only in normoxic conditions. In hypoxic conditions, HIF prolyl-hydroxylase is inhibited, since it utilizes oxygen as a cosubstrate.[20][21]

Inhibition of electron transfer in the succinate dehydrogenase complex due to mutations in the SDHB or SDHD genes can cause a build-up of succinate that inhibits HIF prolyl-hydroxylase, stabilizing HIF-1α. This is termed pseudohypoxia.

HIF-1, when stabilized by hypoxic conditions, upregulates several genes to promote survival in low-oxygen conditions. These include glycolysis enzymes, which allow ATP synthesis in an oxygen-independent manner, and vascular endothelial growth factor (VEGF), which promotes angiogenesis. HIF-1 acts by binding to HIF-responsive elements (HREs) in promoters that contain the sequence NCGTG (where N is either A or G).

It has been shown that muscle A kinase–anchoring protein (mAKAP) organized E3 ubiquitin ligases, affecting stability and positioning of HIF-1 inside its action site in the nucleus. Depletion of mAKAP or disruption of its targeting to the perinuclear (in cardiomyocytes) region altered the stability of HIF-1 and transcriptional activation of genes associated with hypoxia. Thus, "compartmentalization" of oxygen-sensitive signaling components may influence the hypoxic response.[22]

The advanced knowledge of the molecular regulatory mechanisms of HIF1 activity under hypoxic conditions contrast sharply with the paucity of information on the mechanistic and functional aspects governing NF-κB-mediated HIF1 regulation under normoxic conditions. However, HIF-1α stabilization is also found in non-hypoxic conditions through an, until recently, unknown mechanism. It was shown that NF-κB (nuclear factor κB) is a direct modulator of HIF-1α expression in the presence of normal oxygen pressure. siRNA (small interfering RNA) studies for individual NF-κB members revealed differential effects on HIF-1α mRNA levels, indicating that NF-κB can regulate basal HIF-1α expression. Finally, it was shown that, when endogenous NF-κB is induced by TNFα (tumour necrosis factor α) treatment, HIF-1α levels also change in an NF-κB-dependent manner.[23] HIF-1 and HIF-2 have different physiological roles. HIF-2 regulates erythropoietin production in adult life.[24]

الإصلاح وإعادة التولد

In normal circumstances after injury HIF-1a is degraded by prolyl hydroxylases (PHDs). In June 2015, scientists found that the continued up-regulation of HIF-1a via PHD inhibitors regenerates lost or damaged tissue in mammals that have a repair response; and the continued down-regulation of Hif-1a results in healing with a scarring response in mammals with a previous regenerative response to the loss of tissue. The act of regulating HIF-1a can either turn off, or turn on the key process of mammalian regeneration.[25][26]


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كهدف علاجي

الأنيميا

Recently, several drugs that act as selective HIF prolyl-hydroxylase inhibitors have been developed.[27][28] The most notable compounds are: Roxadustat (FG-4592);[29] Vadadustat (AKB-6548),[30] Daprodustat (GSK1278863),[31] Desidustat (ZYAN-1),[32] and Molidustat (Bay 85-3934),[33] all of which are intended as orally acting drugs for the treatment of anemia.[34] Other significant compounds from this family, which are used in research but have not been developed for medical use in humans, include MK-8617,[35] YC-1,[36] IOX-2,[37] 2-methoxyestradiol,[38] GN-44028,[39] AKB-4924,[40] Bay 87-2243,[41] FG-2216[42] and FG-4497.[43] By inhibiting prolyl-hydroxylase enzyme, the stability of HIF-2α in the kidney is increased, which results in an increase in endogenous production of erythropoietin.[44] Both FibroGen compounds made it through to Phase II clinical trials, but these were suspended temporarily in May 2007 following the death of a trial participant taking FG-2216 from fulminant hepatitis (liver failure), however it is unclear whether this death was actually caused by FG-2216. The hold on further testing of FG-4592 was lifted in early 2008, after the FDA reviewed and approved a thorough response from FibroGen.[45] Roxadustat, vadadustat, daprodustat and molidustat have now all progressed through to Phase III clinical trials for treatment of renal anemia.[29][30][31]

الالتهاب والسرطان

In other scenarios and in contrast to the therapy outlined above, recent research suggests that HIF induction in normoxia is likely to have serious consequences in disease settings with a chronic inflammatory component.[46][47][48] It has also been shown that chronic inflammation is self-perpetuating and that it distorts the microenvironment as a result of aberrantly active transcription factors. As a consequence, alterations in growth factor, chemokine, cytokine, and ROS balance occur within the cellular milieu that in turn provide the axis of growth and survival needed for de novo development of cancer and metastasis. These results have numerous implications for a number of pathologies where NF-κB and HIF-1 are deregulated, including rheumatoid arthritis and cancer.[49][50][51][52] Therefore, it is thought that understanding the cross-talk between these two key transcription factors, NF-κB and HIF, will greatly enhance the process of drug development.[23][53]

HIF activity is involved in angiogenesis required for cancer tumor growth, so HIF inhibitors such as phenethyl isothiocyanate and Acriflavine[54] are (since 2006) under investigation for anti-cancer effects.[55][56][57]

علم الأعصاب

Research conducted on mice suggests that stabilizing HIF using an HIF prolyl-hydroxylase inhibitor enhances hippocampal memory, likely by increasing erythropoietin expression.[58] HIF pathway activators such as ML-228 may have neuroprotective effects and are of interest as potential treatments for stroke and spinal cord injury.[59][60]

انظر أيضاً

المراجع

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وصلات خارجية

  • MeSH Hypoxia-Inducible+Factor+1
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Hypoxia-inducible factor 1-alpha
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Aryl hydrocarbon receptor nuclear translocator
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Endothelial PAS domain-containing protein 1
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Hypoxia-inducible factor 3-alpha


قالب:Transcription factors

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