The neuromuscular junction (NMJ) is widely studied for its utility in investigating
synaptic properties and processes and neuromuscular changes in response to injury,
aging, and disease. The NMJ consists of three essential anatomic components, the pre-synaptic
motor axon terminal, the post-synaptic nicotinic acetylcholine receptors (AchRs) on
the muscle, and the perisynaptic Schwann cell (PSC), also known as the terminal Schwann
cell, that caps the synapse (
Figure 1A
). In addition to this tri-partite construction, another cell called the kranocyte
is known to be involved in the structural makeup of the NMJ though even less is known
about this cell type. The PSC is a protective cellular covering for the NMJ and serves
various dynamic functions under normal and pathological conditions. The NMJ is a complex
multi-component site of communication between motor axons and target musculature.
The PSC is a specialized non-myelinating Schwann cell that protects, nourishes, and
regulates synaptic function at the NMJ (Alvarez-Suarez et al., 2020). A dynamic reciprocal
communication network exists between the PSC and muscle to adapt to and help modulate
alterations to NMJ activity in healthy adults. The PSC produces and secretes trophic
factors that influence the axon’s health, post-synaptic muscle, and overall integrity
of the NMJ. Likewise, muscle also secretes trophic factors and other chemical mediators
that influence the PSC and associated localized structures at the NMJ.
Figure 1
NG2 and TBX21 expression improves the ability to study normal and pathological responses
of PSCs at the NMJ.
(A) Co-localization between the Schwann cell marker S100-EGFP and newly discovered
markers NG2 and TBX21 in PSCs could enhance isolation and analysis of various biological
processes in the healthy NMJ. (B) Their role in guiding regenerating axons to reinnervate
the NMJ post-injury. Specific transcription and translational changes in PSCs in response
to nerve injury and axon regeneration are of particular interest. AchRs: Acetylcholine
receptors; EGFP: enhanced green fluorescent protein; FACS/MACS: fluorescence/magnetic
activated cell sorting; GFAP: glial-fibrillary acidic protein; GPR126: G-coupled protein
receptor 126; LCMD: laser capture microdissection; NG2: neural-glial antigen-2; NMJ:
neuromuscular junction; PSCs: perisynaptic Schwann cell; TBX21: T-Box transcription
factor 21. Created with BioRender.com.
These interactions also directly affect PSCs to aid in neuromuscular reinnervation
following nerve injury. Retraction of the motor axon terminals and Wallerian degeneration
of the axonal segments distal to the injury site occurs acutely and rapidly post-injury.
As part of this early response, localized acetylcholine decreases, and the PSC becomes
activated and modifies its biochemistry and morphology. Some changes include an upregulation
of glial fibrillary acidic protein and neuregulin-1/Erb receptor signaling as the
extended cytoplasmic processes of the PSC interact with and guide the regenerating
axon toward its muscular target. Trophic factors and guidance cues produced by activated
PSCs can also directly influence neuromuscular reinnervation (
Figure 1B
). The result is PSC-facilitated reinnervation and reestablishment of the NMJ. Expression
of G-coupled protein receptor, GPR126, by PSCs improves the ability of axons to successfully
reinnervate NMJs after injury, with evidence suggesting it affects trophic factor
production and influences target skeletal muscle chemokine and inflammatory response
(Jablonka-Shariff et al., 2020). However, the extent of GPR126 expression fluctuations
in PSCs over time post-injury is unclear. The correlation between its expression and
changes in other components of the NMJ that influence regenerating motor axon innervation
requires further investigation (
Figure 1B
).
In neuromuscular diseases such as amyotrophic lateral sclerosis (ALS), pre-symptomatic
denervation of skeletal muscle occurs, and early PSC changes are also observed. As
demonstrated by Carrasco et al. (2016) a mouse model of ALS exhibits fewer PSCs at
the NMJ than their wild-type counterparts. The PSCs that are present are misaligned
with the post-synaptic AchRs under normal conditions (Carrasco et al., 2016). This
disorganization of PSCs varies in different muscles. Those exhibiting early pre-symptomatic
PSC abnormalities are more likely to be affected by the onset of denervation of motor
axons from the NMJ in later stages of disease progression. Evidence to date has clearly
shown relevance for PSC presence, reactivity, and morphologic alteration in innervated,
denervated, and reinnervated states of the NMJ.
Despite the increasingly clear importance of the PSC in NMJ integrity and function,
it has remained surprisingly challenging to study the PSC as an individual cell type.
This difficulty has been due in no small part to the fact that PSCs are closely associated
with other structures at the NMJ, making them hard to separate, and they express many
of the same markers as other SCs, including S100 (Jablonka-Shariff et al., 2021).
As such, specific markers for PSCs have not been easily identifiable. Though some
markers and labeling methods for PSCs have been previously identified, such as peanut
agglutinin and monoclonal antibody 2A12 labeling (Astrow et al., 1998), it is necessary
to understand better the development, normal and pathological functions of PSCs. To
do this, clearer and more consistently evident markers of PSCs are needed. A few have
been identified, with two recent advancements highlighting specific proteins that
could aid in efforts to progress PSCs research in health and disease.
Neuron-glial antigen-2 (NG2): Long studied as a marker of glial progenitor cells such
as those of the oligodendrocyte lineage (McTigue et al., 2006), NG2 proteoglycan,
also known as chondroitin sulfate proteoglycan 4, has recently been shown to be expressed
by PSCs at the NMJ (Castro et al., 2020). By crossing mice with enhanced green fluorescent
protein expressed in S100+ cells (S100-EGFP) with the NG2dsRed mouse, Castro et al.
(2020) were able to identify dual-labeled S100-NG2 positive cells at the motor endplate
on the extensor digitorum longus muscle under normal physiologic conditions. Importantly,
co-labeling these fluorescently labeled proteins did not present any adverse outcomes
for PSC morphology or behavior. The group further determined retention of this marker
combination under conditions of stress. A nerve crush injury was performed, and the
co-expression of S100-EGFP and NG2dsRed was maintained at the NMJ, despite clear denervation
observed as early as one day post-injury.
This approach affords the ability to track and better understand the PSCs changes
that occur following denervation. In addition, correlations of other morphological
and protein expression changes at the NMJ can be determined, such as associations
between PSC-morphology change and AchR cluster organization. The reliability of fluorescent
co-labeling of S100-GFP and NG2dsRed of the PSC also allows for biochemical and genetic
analysis through fluorescent-assisted cell sorting under normal and pathologic conditions.
The high expression of NG2 in PSCs brings up interesting questions concerning therapeutic
effects in nerve injury and neuromuscular diseases and where the mechanism of action
could be. Could NG2 be involved in some of the benefits observed through trophic factor
therapy? For example, NG2 has been shown to bind trophic factors PDGF-A and FGF2,
and such factors are components of multifactorial treatments such as stem cell-conditioned.
The identification of NG2 as a marker in PSCs sheds light on possible peripheral therapeutic
target effects and highlights the PSC as a structure of interest in investigating
such therapeutic mechanisms. Many new questions can now be posed concerning PSCs’
specific biochemical and functional actions under normal and pathologic conditions
(
Figure 1
).
T-Box transcription factor 21 (TBX21): TBX21, also known as T-bet, is mainly known
for its roles in lymphocyte and immune cell function, though it has recently been
shown to be expressed in various human body tissues (Zhang et al., 2020). TBX21 is
a transcription factor known to exhibit multiple functions in both the innate and
adaptive arms of the immune system, being expressed in dendritic and natural killer
cells as well as Th1 cells, CD4+ and CD8+T cells, respectively (Lazarevic et al.,
2013). Surprisingly, TBX21 was recently found to be explicitly expressed by PSCs by
Jablonka-Shariff et al. (2021) compared to axonal and muscular components associated
with the NMJ. Like Castro et al. (2020), the S100-EGFP mouse was used, and the fluorescent
NMJ band was isolated from sternocleidomastoid muscle via laser capture microdissection.
The tissue, enriched with fluorescent PSCs, was analyzed by RNA microarray and qT-PCR,
and a list of highly expressed genes was obtained. TBX21 is unique to the PSC and
was expressed over nine times higher than in nerve or muscle tissue. Immunofluorescent
labeling for TBX21 showed clear co-localization with S100-EGFP and alpha-bungarotoxin,
which labels the post-synaptic AchRs.
Though TBX21 research has focused chiefly on immune responses, such responses can
be critical in instigating or progressing inflammatory conditions or disease (Lazarevic
and Glimcher, 2011). Given that neuromuscular diseases, including amyotrophic lateral
sclerosis (ALS), have been linked to inflammatory and immune-associated responses
at the level of the neuron and NMJ (Nardo et al., 2018), the expression of TBX21 in
PSCs could be significant in its regulation of such processes. Though CD8+T cells
are often associated with cytotoxic effects, the major immunohistocompatibility complex
I protein triggered by CD8+T cells appears to be protective of NMJ innervation in
some muscles in a SOD1G93A mouse model of ALS (Nardo et al., 2018). What role TBX21
may play in this response is not clear, but the finding of this PSC-specific marker
at the NMJ will aid studies to elucidate this and many more questions that have remained
unanswered.
Impact on future research: The PSC is a functionally important participant in the
maintenance and plasticity of the NMJ, and these recent studies have highlighted specific
markers to study them more clearly and deeply than previously possible. However, the
physical and physiologic characteristics of the PSC revealed thus far have only begun
to address questions that now may be addressed using these new approaches. A key benefit
for these advances is an improved understanding of the role of the PSC in neuromuscular
denervation and reinnervation under pathologic or therapeutic conditions.
Neuromuscular disconnection represents an early anatomical pre-symptomatic peripheral
pathology in ALS. The loss of NMJ innervation through axon die-back occurs before
axonal degeneration. For example, in the mutant superoxide dismutase 1 G93A (mSOD1G93A)
mouse models of ALS, NMJ endplate denervation is observed approximately seven weeks
into the mouse lifespan. By comparison, symptoms onset occurs at about 14–15 weeks
of age. In slower progressing models, such as the mSOD1G37R mouse, functional PSC
alterations are observed much earlier than morphologic fluctuations. Specifically,
PSC excitability is elevated pre-symptomatically and progressing throughout the lifespan
of the mouse despite sustained structural integrity (breakdown of soleus NMJs in the
G37R model occurs at approximately 55 weeks of age) (Arbour et al., 2015). This pronounced
and prolonged neuromuscular endurance of excitability correlated with motor neuron
hyperexcitability associated with motor neuron degeneration in ALS.
Thus, the PSC functional properties support dysfunctional neuromuscular motor signaling
and promote progressive motor neuron pathology as integrity is broken down later in
the disease. Pre-symptomatic loss of NMJ innervation is also observed in sporadic
and some forms of hereditary ALS in humans. Despite two decades worth of research
into the dying-back phenomenon of motor axons in ALS, the PSC response has remained
relatively understudied. Recently, more findings have shed light on the anatomical
and biological changes that the PSC undergoes following NMJ denervation in ALS. With
the discovery that NG2 and TBX21 can help identify and isolate PSCs, many unanswered
and new questions can be addressed to establish a stronger foundation of knowledge
concerning the role of PSCs in normal conditions and disease.
This work was supported by the United States Department of Veterans Affairs, No. IK2RX002688,
to CLW.