# Role of Activating Transcription Factor 4 in Metabolic, Neurologic, and Ocular Diseases

**Authors:** Minwoo Kwon, Anisha Kasi, Stefan Y. Kim, Arya Bairat, Aidan Kumar, Varun Kumar

PMC · DOI: 10.3390/cells15060538 · 2026-03-18

## TL;DR

This paper reviews how the protein ATF4 helps cells handle stress but can also cause diseases like metabolic disorders, neurological issues, and eye problems.

## Contribution

The paper synthesizes ATF4's dual role in disease and protection, offering insights into its context-dependent effects and therapeutic potential.

## Key findings

- ATF4 activation can both protect cells and induce apoptosis under stress.
- ATF4 is involved in metabolic dysfunction, neurodegenerative diseases, and ocular pathologies.
- The study highlights ATF4's potential as a therapeutic target across multiple disease types.

## Abstract

Cells respond to metabolic and environmental challenges through the integrated stress response (ISR), a cellular process that maintains homeostasis under diverse stressors. ATF4 is a key player in this ISR, as it is activated via the PERK–eIF2α–ATF4 pathway. ATF4 induction can elicit adaptive responses, including the regulation of genes involved in metabolism and autophagy, to maintain homeostasis. However, ATF4 activation can also induce apoptosis, leading to a wide spectrum of diseases, including metabolic, neurologic, and ocular pathologies. This duality reflects the highly context-dependent nature of ATF4 signaling. This review aims to synthesize the role of ATF4 in metabolic dysfunction, neurodegenerative diseases, and ocular pathology; the mechanisms underlying its protective versus pathologic effects; and future directions to refine ATF4’s potential as a clinical therapeutic target across different diseases.

## Linked entities

- **Genes:** ATF4 (activating transcription factor 4) [NCBI Gene 468]
- **Proteins:** ATF4 (activating transcription factor 4), EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3), EIF2A (eukaryotic translation initiation factor 2A)

## Full-text entities

- **Genes:** Eln (elastin) [NCBI Gene 13717] {aka E030024M20Rik}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, Pacs2 (phosphofurin acidic cluster sorting protein 2) [NCBI Gene 217893] {aka 6720425G15Rik, E230011J22, Pacs1l, mKIAA0602}, BBC3 (BCL2 binding component 3) [NCBI Gene 27113] {aka JFY-1, JFY1, PUMA}, Ucp1 (uncoupling protein 1 (mitochondrial, proton carrier)) [NCBI Gene 22227] {aka Slc25a7, Ucp}, TRIB3 (tribbles pseudokinase 3) [NCBI Gene 57761] {aka C20orf97, NIPK, SINK, SKIP3, TRB3}, Eif2ak2 (eukaryotic translation initiation factor 2-alpha kinase 2) [NCBI Gene 19106] {aka 2310047A08Rik, 4732414G15Rik, Pkr, Prkr, Tik}, Eif2ak3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 13666] {aka Pek, Perk}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Lonp1 (lon peptidase 1, mitochondrial) [NCBI Gene 74142] {aka 1200017E13Rik, LON, Prss15}, DDIT3 (DNA damage inducible transcript 3) [NCBI Gene 1649] {aka AltDDIT3, C/EBPzeta, CEBPZ, CHOP, CHOP-10, CHOP10}, EIF2A (eukaryotic translation initiation factor 2A) [NCBI Gene 83939] {aka CDA02, EIF-2A, MST089, MSTP004, MSTP089}, Ddit3 (DNA-damage inducible transcript 3) [NCBI Gene 29467] {aka CHOP, CHOP-10, Chop10, Gadd153, RM4}, Ddit3 (DNA-damage inducible transcript 3) [NCBI Gene 13198] {aka AltDDIT3, CHOP-10, CHOP10, chop, gadd153}, Mfn2 (mitofusin 2) [NCBI Gene 170731] {aka D630023P19Rik, Fzo}, ATF4 (activating transcription factor 4) [NCBI Gene 468] {aka CREB-2, CREB2, TAXREB67, TXREB}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, PRKN (parkin RBR E3 ubiquitin protein ligase) [NCBI Gene 5071] {aka AR-JP, LPRS2, PARK2, PDJ}, Kmt2a (lysine (K)-specific methyltransferase 2A) [NCBI Gene 214162] {aka 6430520K01, ALL-1, All1, Cxxc7, HRX, HTRX1}, Atf4 (activating transcription factor 4) [NCBI Gene 11911] {aka Atf-4, C/ATF, CREB-2, CREB2, TAXREB67}, PINK1 (PTEN induced kinase 1) [NCBI Gene 65018] {aka BRPK, PARK6}, Bbc3 (BCL2 binding component 3) [NCBI Gene 170770] {aka PUMA, PUMA/JFY1}, Bcl2 (B cell leukemia/lymphoma 2) [NCBI Gene 12043] {aka Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik}, CREB3L2 (cAMP responsive element binding protein 3 like 2) [NCBI Gene 64764] {aka BBF2H7}, Opa1 (OPA1, mitochondrial dynamin like GTPase) [NCBI Gene 74143] {aka 1200011N24Rik, lilr3, mKIAA0567}, EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 9451] {aka PEK, PERK, WRS}
- **Diseases:** Ocular Disease (MESH:D005128), fibrosis (MESH:D005355), ocular hypertension glaucoma (MESH:D009798), cerebral ischemia (MESH:D002545), Metabolic Disease (MESH:D008659), ischemic injury (MESH:D017202), pulmonary fibrosis (MESH:D011658), memory impairment (MESH:D008569), neuronal (MESH:D009410), TBI (MESH:D000070642), inflammation (MESH:D007249), neuronal apoptosis (MESH:D065703), hyperglycemia (MESH:D006943), AD (MESH:D000544), neuronal necrosis (MESH:D009336), disease (MESH:D004194), ventricular dysfunction (MESH:D018754), retinal ganglion (MESH:D012173), Glaucoma (MESH:D005901), middle cerebral artery occlusion (MESH:D020244), abdominal aortic aneurysm (MESH:D017544), injury to (MESH:D014947), lung disease (MESH:D008171), , neurological, and ocular diseases (MESH:D020271), Retinopathy (MESH:D058437), COPD (MESH:D029424), diabetes (MESH:D003920), CIRI (MESH:D015427), mitochondrial dysfunction (MESH:D028361), neurodegeneration (MESH:D019636), Metabolic, Neurologic, and Ocular Diseases (MESH:D001928), toxicity (MESH:D064420), neuroinflammation (MESH:D000090862), PD (MESH:D010300), cognitive impairment (MESH:D003072), FECD (MESH:D005642), Neurotoxicity (MESH:D020258)
- **Chemicals:** DEHP (MESH:D004051), NAD+ (MESH:D009243), glucose (MESH:D005947), Palmitate (MESH:D010168), adaptaquin (MESH:C000705890), Fatty acid (MESH:D005227), squalene (MESH:D013185), calcium (MESH:D002118), creatine (MESH:D003401), ISRIB (-), tunicamycin (MESH:D014415), triglyceride (MESH:D014280), silicone oil (MESH:D012827), NADPH (MESH:D009249), nicotinamide mononucleotide (MESH:D009537), GSK2606414 (MESH:C576403)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Human papillomavirus 16 (serotype) [taxon 333760], Mus musculus (house mouse, species) [taxon 10090], Drosophila melanogaster (fruit fly, species) [taxon 7227], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481), ARPE-19 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0145)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13025863/full.md

---
Source: https://tomesphere.com/paper/PMC13025863