Floundering motor neurons rely on a support network for help, and they send out a distress call to astroglia in the form of angiogenin, report the authors of a paper in the April 11 Journal of Neuroscience. Angiogenin, a candidate gene for amyotrophic lateral sclerosis, might be a therapeutic for the disease based on these and other data, propose the authors in the laboratory of Jochen Prehn at the Royal College of Surgeons in Dublin, Ireland. The team describes how stressed motor neurons secrete angiogenin, which astrocytes endocytose. Angiogenin then cleaves astrocyte RNAs, although the precise nature of the genes targeted and the protective response remain to be determined.

Angiogenin mutations that disrupt the protein’s RNase action or cellular location have been associated with both familial and sporadic forms of ALS (see ARF related news story on Greenway et al., 2006) as well as Parkinson’s disease (see ARF related news story on van Es et al., 2011), but it remains unproven as an ALS gene, wrote John Hardy of the University College London, U.K., in an e-mail to ARF (see also Schymick et al., 2007). However, as Prehn noted in an e-mail, biological evidence suggests the protein does play a role in the disease. Angiogenin concentrations are abnormally reduced in the plasma and cerebrospinal fluid of people with ALS (McLaughlin et al., 2010), while it protects motor neurons from excitotoxic insults and serum starvation in vitro. Moreover, treating ALS model mice with angiogenin delays their death (Kieran et al., 2008; see ARF related news story on Li et al., 2011).

In the current work, joint first authors Alexandra Skorupa and Matthew King and colleagues figured out how angiogenin might protect neurons. In immunofluorescence experiments with mouse primary mixed motor neuron cultures, they observed that, while motor neurons possessed endogenous angiogenin, they did not internalize recombinant angiogenin added to the media. Conversely, astrocytes that did not make much angiogenin on their own did take it up, shunting it first into vesicles and then into the nucleus. Based on these data, the team hypothesized that motor neurons produce angiogenin and astroglia internalize it.

In further experiments, the researchers showed that conditioned medium from stressed NSC34 motor neuron-like cells contained angiogenin, and that purified astrocytes took it up. This confirmed the neuron-to-astrocyte signal. To examine the astrocyte-to-neuron response, the team treated mixed cultures with recombinant angiogenin for six hours, washed away the exogenous RNase, then collected the media 18 hours later and tested it on a different mixed culture. They found that the conditioned media protected neurons from toxicity caused by the glutamate agonist AMPA. The authors concluded that angiogenin-treated cultures produce something that protects motor neurons, but they did not investigate what confers that protection.

The researchers did pursue the mechanism of angiogenin uptake. They reasoned that there were two possible entryways: clathrin-mediated or lipid raft-mediated endocytosis. They found that only a clathrin pathway blocker affected angiogenin uptake. The researchers suspected the angiogenin receptor might be syndecan 4, which binds similar angiogenic, neuroprotective factors (Tkachenko et al., 2004). Finding that syndecan 4 and angiogenin co-localize in astrocytes supported their suspicion. That RNA interference for syndecan 4 blocked angiogenin uptake reinforced it.

What does angiogenin do once inside astrocytes? Since the protein cleaves RNAs, Prehn and colleagues examined astrocyte nucleic acids, finding that angiogenin fragmented them. However, the ALS-linked angiogenin mutation lysine-401-isoleucine failed to mediate the nuclease effect. “Angiogenin regulates astroglia function by targeting novel subsets of RNAs,” the researchers concluded in the paper, noting that “future studies will need to identify and characterize these novel angiogenin substrates.” The researchers are currently exploring the relevant RNAs, Prehn wrote in an e-mail to ARF. They are also partnering with a company to develop angiogenin as a therapy, he wrote.—Amber Dance

Comments

  1. The manuscript identifies a novel role of angiogenin, a member of the pancreatic RNase A superfamily, in communication between neurons and glia in the spinal cord. Mutations in angiogenin are associated with amyotrophic lateral sclerosis; therefore, its functions in the spinal cord are of great importance. Authors propose that angiogenin is secreted from motor neurons upon stress and internalized by astrocyte cultures, such that its RNase activity has a paracrine effect on astroglia. Whereas the authors demonstrate increased RNA cleavage upon serum withdrawal in astroglia, the identity of the cleaved RNAs and the direct role of angiogenin in the cleavage are still unclear. However, the authors provide substantial evidence for a role of clathrin-dependent vesicle transport and syndecan-4 receptor in angiogenin internalization by astrocytes. Importantly, such paracrine function of angiogenin creates new opportunities for neuroprotective therapies.

    View all comments by Jernej Ule

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References

News Citations

  1. ALS—Study Strengthens VEGF Connection, Potential Biomarkers Proffered
  2. A Fork in the Road: Angiogenin Predisposes to ALS and Parkinson’s
  3. Trichostatin A, Angiogenin Keep Neurons Alive in ALS

Paper Citations

  1. . ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nat Genet. 2006 Apr;38(4):411-3. PubMed.
  2. . Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol. 2011 Dec;70(6):964-73. PubMed.
  3. . Genetics of sporadic amyotrophic lateral sclerosis. Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R233-42. PubMed.
  4. . Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosis. PLoS One. 2010;5(11):e15402. PubMed.
  5. . Control of motoneuron survival by angiogenin. J Neurosci. 2008 Dec 24;28(52):14056-61. PubMed.
  6. . Angiogenin inhibits nuclear translocation of apoptosis inducing factor in a Bcl-2-dependent manner. J Cell Physiol. 2011 Jun 15; PubMed.
  7. . Fibroblast growth factor 2 endocytosis in endothelial cells proceed via syndecan-4-dependent activation of Rac1 and a Cdc42-dependent macropinocytic pathway. J Cell Sci. 2004 Jul 1;117(Pt 15):3189-99. PubMed.

Further Reading

Papers

  1. . Decreased serum angiogenin level in Alzheimer's disease. Prog Neuropsychopharmacol Biol Psychiatry. 2012 Mar 15; PubMed.
  2. . Mechanisms of loss of functions of human angiogenin variants implicated in amyotrophic lateral sclerosis. PLoS One. 2012;7(2):e32479. PubMed.
  3. . Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort. Amyotroph Lateral Scler. 2012 May;13(3):270-5. PubMed.
  4. . Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation. Acta Neuropathol. 2009 Oct;118(4):561-73. PubMed.
  5. . Angiogenin-mediated rRNA transcription in cancer and neurodegeneration. Int J Biochem Mol Biol. 2010;1(1):26-35. PubMed.
  6. . Human angiogenin presents neuroprotective and migration effects in neuroblastoma cells. Mol Cell Biochem. 2010 Jul;340(1-2):133-41. PubMed.

Primary Papers

  1. . Motoneurons secrete angiogenin to induce RNA cleavage in astroglia. J Neurosci. 2012 Apr 11;32(15):5024-38. PubMed.