Autophagosome

Autophagosome formation is initiated by assembly and recruitment of the core autophagy machinery to distinct cellular sites, known as phagophore assembly sites (PAS) in yeast or autophagosome formation sites in other organisms. The process is tightly regulated by multiple autophagy-related (ATG) proteins.{{Cite journal |last1=Hollenstein |first1=David M. |last2=Kraft |first2=Claus |date=August 2020 |title=Autophagosomes are formed at a distinct cellular structure |journal=Current Opinion in Cell Biology |volume=65 |pages=50–57 |doi=10.1016/j.ceb.2020.02.012 |pmc=7588827 |pmid=32203894}}

The ULK1/ATG1 complex is the initial activator of autophagy in response to nutrient starvation, and it recruits other ATG proteins to the PAS. The class III phosphatidylinositol 3-kinase (PI3K) complex, including VPS34 and Beclin-1, produces phosphatidylinositol 3-phosphate (PI3P), which is essential for phagophore membrane dynamics. Membrane sources for phagophore expansion may include the endoplasmic reticulum, mitochondria, Golgi apparatus, and recycling endosomes.

After the formation of the spherical structure, ATG12-ATG5:ATG16L1 or E3-like complex (E3 for short) acts as a ubiquitin-like E3 enzyme, promoting LC3/GABARAP proteins anchoring to the AP membrane.{{Cite journal |last1=Iriondo |first1=Marina N. |last2=Etxaniz |first2=Asier |last3=Varela |first3=Yaiza R. |last4=Ballesteros |first4=Uxue |last5=Lázaro |first5=Melisa |last6=Valle |first6=Mikel |last7=Fracchiolla |first7=Dorotea |last8=Martens |first8=Sascha |last9=Montes |first9=L. Ruth |last10=Goñi |first10=Félix M. |last11=Alonso |first11=Alicia |date=2023-02-02 |title=Effect of ATG12–ATG5-ATG16L1 autophagy E3-like complex on the ability of LC3/GABARAP proteins to induce vesicle tethering and fusion |journal=Cellular and Molecular Life Sciences |language=en |volume=80 |issue=2 |doi=10.1007/s00018-023-04704-z |issn=1420-682X |pmc=9894987 |pmid=36729310}}

LC3 is cleaved by ATG4 protease to generate cytosolic LC3. The cleavage is required for the terminal fusion of an autophagosome with its target membrane. LC3 is cleaved and lipidated to form LC3-II,which associates with the autophagosomal membraneand is used as a marker of autophagosomes in immunocytochemistry, because it is the essential part of the vesicle and stays associated until the last moment before its fusion. At first, autophagosomes fuse with endosomes or endosome-derived vesicles and stays associated until the last moment before its fusion.{{Cite journal |last1=Runwal |first1=Gautam |last2=Stamatakou |first2=Eleanna |last3=Siddiqi |first3=Farah H. |last4=Puri |first4=Claudia |last5=Zhu |first5=Ye |last6=Rubinsztein |first6=David C. |date=2019-07-12 |title=LC3-positive structures are prominent in autophagy-deficient cells |journal=Scientific Reports |language=en |volume=9 |issue=1 |pages=10147 |doi=10.1038/s41598-019-46657-z |pmid=31300716 |pmc=6625982 |bibcode=2019NatSR...910147R |issn=2045-2322}}

After the phagophore fully encloses its cargo, it seals and becomes a mature autophagosome. This structure then fuses with lysosomes to form an autolysosome, where the contents are degraded and recycled.

This process is similar in yeast, however the gene names differ. For example, LC3 in mammals is Atg8. In yeast autophagosomes are generated from [https://pmc.ncbi.nlm.nih.gov/articles/PMC2366851/ Pre-Autophagosomal Structure (PAS)] which is distinct from the precursor structures in mammalian cells. The pre-autophagosomal structure in yeast is described as a complex localized near the vacuole. However the significance of this localization is not known. Mature yeast autophagosomes fuse directly with vacuoles or lysosomes, and do not form [https://pmc.ncbi.nlm.nih.gov/articles/PMC8935502/ amphisomes] as in mammals. In yeast autophagosome maturation, there are also other known players such as Atg1, Atg13 and Atg17. Atg1 is a kinase upregulated upon induction of autophagy. Atg13 regulates Atg1 and together they form a complex called Atg13:Atg1, which receives signals from the master of nutrient sensing – Tor. Atg1 is also important in late stages of autophagosome formation.{{cite journal |last=Reggiori |first=F. |author2=Klionsky D.J. |date=2013 |title=Autophagic process in Yeast: Mechanisms, Machinery and Regulation |journal=Genetics |volume=194 |issue=2 |pages=341–361 |doi=10.1534/genetics.112.149013 |pmc=3664846 |pmid=23733851}}

In neurons, autophagosomes are generated at the neurite tip and mature (acidify) as they travel towards the cell body along the axon.{{Cite journal|last1=Maday|first1=S|last2=Wallace|first2=K. E.|last3=Holzbaur|first3=E. L.|author-link3=Erika Holzbaur|year=2012|title=Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons|journal=The Journal of Cell Biology|volume=196|issue=4|pages=407–17|doi=10.1083/jcb.201106120|pmc=3283992|pmid=22331844}} This axonal transport is disrupted if huntingtin or its interacting partner HAP1, which colocalize with autophagosomes in neurons, are depleted.{{Cite journal

| pmid = 24453320

| pmc = 3898289

| year = 2014

| last1 = Wong

| first1 = Y. C.

| title = The regulation of autophagosome dynamics by huntingtin and HAP1 is disrupted by expression of mutant huntingtin, leading to defective cargo degradation

| journal = Journal of Neuroscience

| volume = 34

| issue = 4

| pages = 1293–305

| last2 = Holzbaur

| first2 = E. L.

| doi = 10.1523/JNEUROSCI.1870-13.2014

}}

Autophagosomes serve as essential carriers in the autophagy pathway, enabling cells to adapt to metabolic stress and maintain homeostasis. They are responsible for the selective degradation of damaged organelles (for example, mitophagy (mitochondria), pexophagy (peroxisomes), aggrephagy (protein aggregates), glycophagy (glycogens), lipophagy (lipids), ribophagy (ribosome), xenophagy (pathogens),and ER-phagy).{{Cite journal |last1=Khandia |first1=Ravindra |last2=Dadar |first2=Maryam |last3=Munjal |first3=Ashok |last4=Dhama |first4=Kuldeep |last5=Karthik |first5=Kannan |last6=Tiwari |first6=Rakesh |last7=Yatoo |first7=MI |last8=Iqbal |first8=HMN |last9=Singh |first9=KP |last10=Joshi |first10=SK |last11=Chaicumpa |first11=Weerachai |date=2019-07-03 |title=A Comprehensive Review of Autophagy and Its Various Roles in Infectious, Non-Infectious, and Lifestyle Diseases: Current Knowledge and Prospects for Disease Prevention, Novel Drug Design, and Therapy |journal=Cells |volume=8 |issue=7 |pages=674 |doi=10.3390/cells8070674 |doi-access=free |pmc=6678135 |pmid=31277291}}

This selective removal is crucial for cellular quality control, helping prevent the accumulation of toxic proteins and damaged components. Autophagy also plays roles in development, immunity, and cell differentiation. For instance, autophagosomes assist in antigen presentation, regulate inflammatory signaling, and contribute to the elimination of intracellular bacteria and viruses.

Defects in autophagosome function have been linked to several human diseases. In addition to neurodegenerative diseases such as Alzheimer's, Parkinson's, and Huntington's, impaired autophagy is associated with cancer, infectious diseases, and metabolic disorders like type 2 diabetes.{{Cite journal |last1=Levine |first1=B. |last2=Yorimitsu |first2=T. |year=2008 |title=Autophagy in the pathogenesis of disease |journal=Cell |volume=132 |issue=1 |pages=27–42 |doi=10.1016/j.cell.2007.12.018|pmc=2696814 }}

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Category:Cell biology