Proteomic analysis of tears following acupuncture treatment for menopausal dry eye disease by two-dimensional nano-liquid chromatography coupled with tandem mass spectrometry.

BACKGROUND: The purpose of this study was to investigate whether acupuncture is effective at treating dry eye disease among postmenopausal women and to identify the possible mechanisms.
METHODS: Twenty-eight postmenopausal women with dry eye disease were randomly divided into two groups: an acupuncture plus artificial tears (AC + AT) group and an artificial tears (AT) only group. After baseline examination of clinical parameters and tear sample collection, each patient received the designated modality of topical therapy for 2 months. Post-treatment documentation of clinical parameters was recorded, and tear samples were collected. Tear samples from the AC + AT group were subjected to two-dimensional nano-liquid chromatography coupled with tandem mass spectrometry (2D nano-LC-MS/MS). Western blot analysis was also performed on tear samples from both groups.
RESULTS: After treatment, the Ocular Surface Disease Index scores, symptom assessment scores, scores of sign assessment, and tear break-up time were significantly improved in both groups (P=0.000). Symptom assessment scores were significantly improved in the AC + AT group (P=0.000) compared with the AT group. 2D nano-LC-MS/MS identified 2,411 proteins, among which 142 were downregulated and 169 were upregulated. After combined AC + AT treatment, the abundance of secreted proteins was increased, whereas that of cytoplasmic proteins decreased (Pearson's χ2 test, P=0.000, P=0.000, respectively). Proteins involved in immunity and regulation were also more abundant (Pearson's χ2 test, P=0.040, P=0.016, respectively), while components and proliferation-related proteins were downregulated (Pearson's χ2 test, P=0.003, P=0.011, respectively).
CONCLUSION: AC + AT treatment increased protein synthesis and secretion, and improved clinical symptoms. These results indicate that acupuncture may be a complimentary therapy for treating postmenopausal dry eye disease.

RCT Entities:   Population Interventions Outcomes

Introduction

The prevalence of dry eye disease is higher among women than men. Additionally, aging has been identified as a risk factor for this condition, which suggests that hormones may play key roles in the incidence and course of dry eye, especially in postmenopausal women.1 Common treatments for dry eye aim to increase the amount of tears at the ocular surface through the use of tear replacement with artificial tears or to reduce drainage by occlusion of the drainage system.2 However, such treatments are often palliative and inadequate with regard to providing satisfactory relief from debilitating symptoms.3 Hormone replacement therapy may improve aqueous tear production but not the quality of tears in dry eye disease, and the effect on tear production is dependent upon age.4 Nonetheless, recent studies indicate that hormone replacement therapy can increase the risk of coronary heart disease, stroke, and breast and endometrial cancers.5,6

As a complementary alternative therapy without serious side effects, acupuncture is used to treat postmenopausal symptoms including hot flashes,7 burning mouth syndrome, and sleep disturbances. According to recent studies, acupuncture may benefit midterm outcomes related to dry eye syndrome in comparison with artificial tears.8 For example, acupuncture was found to improve the signs and symptoms of dry eye in patients after 4 weeks of treatment.9 However, the effectiveness and mechanisms of acupuncture on postmenopausal dry eye have not yet been reported. In this trial, we aimed to investigate whether acupuncture is effective at treating dry eye among postmenopausal women and to identify the possible mechanisms.

Methods

Subjects

Twenty-eight patients were included in this study (Table 1). All participants were allocated into either an acupuncture plus artificial tears (AC + AT) group or an artificial tears (AT) only group. This research began on September 8, 2014, and lasted for 10 months. Menopausal women over 50 years old who were diagnosed with dry eye (with dry eye symptoms and Schirmer’s test results less than 10 mm/5 minutes or a tear break-up time [TBUT] less than 10 seconds) were eligible to participate in this study. Patients with serious eye disease, inflammation, surgery and trauma, ovariotomy or hysterectomy, and other severe body and mental diseases were excluded. Basic information for every participant was recorded or tested during their first visit, including the following: the symptoms and course of dry eye disease, the eye drops they used prior to enrollment, and the Ocular Surface Disease Index (OSDI), Generalized Anxiety Disorder 7-Item Scale (GAD-7), Patient Health Questionnaire 9-Item (PHQ-9), TBUT, and Schirmer’s test (without narcosis) scores. Venous blood and tears were also collected to detect sex hormones and for tear proteomics and Western blot analyses. The study was approved by the Ethics Committee of Shanghai Tenth People’s Hospital of Tongji University. All patients provided written informed consent to participate in this study.

Table 1

Demographic and baseline characteristics of the study subjects

Characteristics	AC + AT group	AT group	Total
Number	14	14	28
Number of eyes	28	28	56
Age (years)	60.714±3.292	60.786±3.745	60.750±3.460
Disease course (years)	3.857±3.225	3.786±3.011	3.821±3.061
Treatment course (months)	2	2	2

Notes: AC + AT group, acupuncture plus artificial tears; AT group, artificial tears only group. Data presented as n or mean ± standard deviation.

Treatment procedure

The intervention lasted for 2 months. In the AC + AT group, each patient was offered acupuncture treatment, which lasted for 30 minutes each session, three times a week for 8 weeks. The acupuncture treatment, which consisted of the acupoints of Jingming (BL 1), Cuanzhu (BL 2), Sizhukong (SJ 23), Taiyang (EXTRAI), Sibai (ST 2), Hegu (LI 4), Fengchi (GB 20), Baihui (DU 20), and Chengqi (ST 1), was performed by one Chinese medicine physician (Figure 1). Participants in both intervention groups accepted artificial tear treatment. After treatment, their symptoms and OSDI, TBUT, and Schirmer’s test (without narcosis) were recorded again, and venous blood and tears were collected.

Figure 1

Location of the acupuncture points used in the study.

Tear collection

Tears were collected by placing a Schirmer’s test strip over the lower lid, 1/3 from the lateral canthus, without anesthesia. Patients were asked to keep their eyes closed for 5 minutes. After the wet length was recorded, the strip was placed into a 1.5 mL Eppendorf tube. Samples were immediately placed into ice transport tanks and transferred to the center lab at Shanghai Tenth People’s Hospital where they were stored at −80°C.

Protein extraction and labeling with isobaric tags for relative and absolute quantitation (iTRAQ) reagents

Proteins from patients in the AC + AT group pre- and post-treatment were extracted from the Schirmer’s test strip by incubation overnight at 4°C in 1 mL dissolution buffer (SCIEX, 4352135, Framingham, MA, USA). After centrifugation at 13,000 rpm for 10 minutes at 4°C, the supernatant was obtained and concentrated by ultrafiltration through Amicon® Ultra 0.6 mL, 3 kDa filters (Millipore, Billerica, MA, USA). Protein concentrations were measured using a bicinchoninic acid assay Protein Assay Kit (Pierce, Rockford, IL, USA). Then, 200 μg of proteins was incubated with dissolution buffer, 1 μL of 2% sodium dodecyl sulfate (SDS), and 4 μL reducing reagent (SCIEX, 4352135) for 1 hour at 60°C. After centrifugation, the precipitate was incubated with 2 μL cysteine blocking reagent (SCIEX, 4352135) for 10 minutes at room temperature. After reduction and alkylation, each sample was digested with trypsin (w(trypsin):w(protein) = 1:25) overnight at 37°C. The samples were then labeled with iTRAQ reagents (Applied Biosystems, Foster City, CA, USA) as follows: 114/115 iTRAQ reagent for pretreatment samples; 116/117 iTRAQ reagent for posttreatment samples. A total of four different isobaric tags were applied to four pooled protein samples, and each of the four labeled digested samples were mixed.

Two-dimensional liquid chromatography coupled with tandem mass spectrometry (2D nano-LC-MS/MS)

The peptide mixture was diluted 10-fold with water/formic acid (pH 3.0) and loaded onto an strong cation exchange chromatography column (SCIEX, 4326695) and fractionated into ten subgroups using isotope-coded affinity tag Cation Exchange Buffer (SCIEX, 4326747). Each strong cation exchange fraction was desalted using reverse-phase (RP) chromatography.

The fractions were separated by nano-high performance liquid chromatography (Eksigent Technologies, Dublin, CA, USA) using a secondary RP analytical column (Eksigent, C18, 3 μm, 150 mm × 75 μm). Peptides were subsequently eluted using the following gradient conditions: phase B (98% acetonitrile with 0.1% formic acid) from 5% to 45% B (5–100 minutes). The total flow rate was maintained at 300 nL/minute. An electrospray voltage of 2.3 kV vs the inlet of the mass spectrometer was used. An AB SCIEX TripleTOF™ 4600 mass spectrometer (Foster city, CA, USA) was operated in information-dependent data acquisition mode to automatically switch between MS and MS/MS acquisition. MS spectra were acquired across the mass range of 350–1,250 m/z using an accumulation time of 250 ms per spectrum. MS spectra, scanned from 100 to 1,500 m/z in high-sensitivity mode with rolling collision energy, were acquired. The 30 most intense precursors were selected for fragmentation per cycle with a dynamic exclusion time of 25 seconds.

iTRAQ data analysis and statistical analysis

Protein identification and quantification of iTRAQ data were performed using ProteinPilot software version 4.5 (AB SCIEX). The paragon algorithm in ProteinPilot software was used for peptide identification and isoform-specific quantification. The signal from the iTRAQ114 group served as the internal reference for signal intensity to which all signals were normalized. The weighted average of the ratios of the respective peptides was calculated based on the protein quantitation results. False discovery rate analysis was conducted, and the detected protein threshold was set to <0.01. The proteomic database used in this study was for Homo sapiens (UniProKB) (http://www.uniprot.org/uniprot).

The differentially expressed proteins were set as follows: ≥1.2 indicating upregulated (P<0.05) and ≤0.8 indicating downregulated (P<0.05).

Western blot analysis

To confirm the 2D nano-LC-MS/MS findings, Western blot analysis of the following proteins was performed on tear samples from both groups: Annexin A1 and apolipoprotein A-I (Apo A-I). The Schirmer’s test strips for eight patients within each group were analyzed. For tear fluid extraction, the test strips were incubated in buffer (200 μL buffer containing 180 μL phosphate buffer saline and 20 μL protease inhibitor) for 24 hours at 4°C followed by centrifugation at 12,000 rpm for 30 minutes. The centrifugal force pulled the tear fluid out of the strip into the buffer. The protein concentrations were measured using an assay based on the Bradford procedure (Bio-Rad, Hercules, CA, USA). Total proteins (30 μg) were then analyzed using Western blotting, resolution via reducing 15% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and electrophoretic transfer onto 0.1 μm pore size nitrocellulose membranes at room temperature for 1 hour at 0.8 mA/cm2. Bands were detected with a primary antibody against Annexin A1 (rabbit-anti-Annexin A1, 1:1,000, #3299, Cell Signaling Technology, Danvers, MA, USA) or ApoA1 (mouse-anti-ApoA1, 1:1,000, #3350, Cell Signaling Technology) followed by incubation with the secondary antibody (anti-rabbit IgG, 1:1,000, #5174, Cell Signaling Technology). The molecular weights of the detected protein bands were estimated using protein standards (Prestained Protein Ladder, Fermentas, Waltham, MA, USA) ranging from 10 to 170 kDa.

Statistical analysis

v2 tests, Student’s t-tests, and Pearson’s χ2 tests were performed using SPSS statistical software 24.0 (IBM Corporation, Armonk, NY, USA). P≤0.05 was considered significant.

Results

Changes in clinical outcomes

Clinical parameters

After treatment, OSDI scores, symptom assessment scores, scores of sign assessment, and TBUT scores were significantly improved in both groups (P=0.000). Conversely, Schirmer’s test results were unchanged in both groups. Compared with the AT group, symptom assessment scores were significantly improved in the AC + AT group (P=0.000), though there were no significant differences between the two groups with regard to the other clinical parameters (Table 2).

Table 2

Changes of clinical parameters

Clinical parameters	AC + AT group			AT group			P-value*
	Pretreatment	Posttreatment	P-value	Pretreatment	Posttreatment	P-value
OSDI scores	48.83±17.68	24.55±17.43	0.000	51.41±16.25	39.08±18.68	0.002	0.043
Scores of symptom	10.07±1.84	4.68±2.54	0.000	10.29±1.82	7.43±2.08	0.000	0.000
Scores of sign	15.07±2.69	11.21±2.96	0.000	14.00±2.71	11.46±2.29	0.000	0.725
TBUT	2.64±1.49	4.57±2.71	0.000	1.93±1.30	4.75±1.74	0.000	0.770
Schirmer’s test	4.93±3.39	5.89±4.51	0.362	4.86±2.52	5.43±2.91	0.277	0.649

Notes: AC + AT group, acupuncture plus artificial tears; AT group, artificial tears only group. Data presented as mean ± standard deviation.

Comparison between post treatment of AC+AT and AT group.

Abbreviations: OSDI, Ocular Surface Disease Index; TBUT, tear break-up time.

Sex hormone levels

After treatment, the levels of follicle-stimulating hormone and luteinizing hormone were increased (65.59±20.08 vs 60.302±17.831 and 28.262±9.251 vs 25.389±6.822, respectively), though the differences were not statistically significant (P=0.132 and P=0.129, respectively). Levels of testosterone were 0.23±0.18 vs 0.27±0.21 (P=0.302), and those of progesterone were 0.582±0.323 vs 0.628±0.347 (P=0.354). Estradiol levels in both groups were <18 pmol/L, which was not significantly different after treatment.

iTRAQ analysis of tear proteins

A total of 2,411 proteins were successfully identified in the iTRAQ analysis, among which 142 proteins were downregulated and 169 proteins were upregulated. To characterize the molecular features of tear proteins that exhibited alterations after treatment, subcellular location and functional categories were investigated (Figure 2A and B). Among the downregulated proteins, cytoplasmic (44.37%), secreted (10.56%), membrane, and other (both 8.45%) proteins comprised the top categories. The top three categories of upregulated proteins were secreted (28.99%), cytoplasmic (24.26%), and other proteins (15.38%). Functional category analysis showed that proteins involved in metabolism (33.80%), binding (14.79%), and cell components (13.38%) were among the top three types of downregulated proteins. The top three categories of upregulated protein functions were metabolism (31.36%), immunity (18.93%), and binding (11.83%).

Figure 2

Integrated analyses of proteome data from tear fluid after AC + AT treatment.

Notes: (A) The subcellular location of down/upregulated proteins is identified. (B) The function of down/upregulated proteins is identified. Comparison of the downregulated and upregulated proteins (Pearson’s χ2, *P<0.05, **P<0.01). AC + AT group, acupuncture plus artificial tears; AT group, artificial tears only group.

Abbreviation: NA, no annotation.

The percentage and constituent ratios of the regulated proteins are shown in Table 3. After AC + AT treatment, secreted proteins were upregulated, and those residing in the cytoplasm were downregulated (Pearson’s χ2 test, P=0.000, P=0.000, respectively). In addition, proteins involved in immunity, regulation, and no annotation were upregulated (Pearson’s χ2 test, P=0.040, P=0.016, P=0.037, respectively), whereas cell components and proliferation-related proteins were downregulated (Pearson’s χ2 test, P=0.003, P=0.011, respectively).

Table 3

The percentage and constituent ratios of regulated proteins

	Downregulated		Upregulated		P-value
Location
Secreted	15	10.56%	49	28.99%	0.000
Cytoplasm	63	44.37%	41	24.26%	0.000
Others	12	8.45%	26	15.38%	0.063
Nucleus	8	5.63%	17	10.06%	0.153
Membrane	12	8.45%	11	6.51%	0.515
Cell junction	2	1.41%	3	1.78%	0.798
NA	30	21.13%	22	13.02%	0.056
Function
Components	19	13.38%	7	4.14%	0.003
Proliferation	11	7.75%	3	1.78%	0.011
Regulation	2	1.41%	12	7.10%	0.016
Immunity	15	10.56%	32	18.93%	0.040
Apoptosis	12	8.45%	6	3.55%	0.065
Transduction	1	0.70%	5	2.96%	0.150
Transporting	5	3.52%	11	6.51%	0.235
Binding	21	14.79%	20	11.83%	0.443
Metabolism	48	33.80%	53	31.36%	0.647
Coagulation	3	2.11%	4	2.37%	0.880
NA	5	3.52%	16	9.47%	0.037

Abbreviation: NA, no annotation.

The regulated ratio was altered by more than 50%. To identify significantly regulated proteins, of which the location and functional categories are shown in Table 4, the downregulated ratio was set to <0.5, and the upregulated ratio was set to>2. These proteins included those involved in the inflammatory reaction and immune response such as polymeric immunoglobulin receptor and Apo A-I, apoptosis-related proteins such as Annexin A1 and aldehyde dehydrogenase, and cell components and metabolism-related proteins such as myosin-14 and neuroblast differentiation-associated protein AHNAK.

Table 4

The location and function categories of significantly regulated proteins

Accession	Name	Ratio	Location	Function
Downregulated
P01833	P01833 polymeric immunoglobulin receptor	0.13	Secreted	Immunity
Q7Z406	Myosin-14	0.23	NA	Binding
Q09666	Neuroblast differentiation-associated protein AHNAK	0.23	Cytoplasm	Proliferation/differentiation
P04083	Annexin A1	0.25	NA	Apoptosis
P30740	Leukocyte elastase inhibitor	0.26	Nucleus	Immunity
P04792	Heat shock protein β-1	0.26	Cell junction	Apoptosis
P06702	Protein S100-A9	0.28	Secreted	Immunity
Q99935	Proline-rich protein 1	0.35	Secreted	Binding
O75556	Mammaglobin-B	0.35	NA	Cell components
Q562R1	β-Actin-like protein 2	0.35	NA	Metabolism
Q13813	Spectrin α chain, non-erythrocytic 1	0.38	Cytoplasm	Metabolism
P17931	Galectin-3	0.40	Cytoplasm	Immunity
P35579	Myosin-9	0.41	Secreted	Binding
P07355	Annexin A2	0.41	NA	Apoptosis
P08727	Keratin, type I cytoskeletal 19	0.41	Cytoplasm	Cell components
P31947	14-3-3 protein σ	0.42	Membrane	Binding
P13797	Plastin-3	0.43	Nucleus	Binding
P01037	Cystatin-SN	0.43	Secreted	Metabolism
Q9UGM3	Deleted in malignant brain tumors 1 protein	0.44	Secreted	Immunity
P80303	Nucleobindin-2	0.44	NA	Binding
P80748	Ig λ-chain V-III region LOI	0.44	NA	Immunity
P05109	Protein S100-A8	0.45	NA	Immunity
P27348	14-3-3 protein θ	0.45	Cytoplasmic	Binding
Q92817	Envoplakin	0.47	Secreted	Transporting
P19013	Keratin, type II cytoskeletal 4	0.47	Cytoplasm	Proliferation/differentiation
Q14204	Cytoplasmic dynein 1 heavy chain 1	0.49	Cytoplasm	Metabolism
Q9BUF5	Tubulin β-6 chain	0.49	Cytoplasm	Proliferation/differentiation
Upregulated
P01024	Complement C3	3.16	Secreted	Immunity
P01857	Ig γ-1 chain C region	3.02	Secreted	Immunity
P02787	Serotransferrin	2.88	Secreted	Transporting
P10909	Clusterin	2.81	Secreted	Apoptosis
P00450	Ceruloplasmin	2.81	Cytoplasm	Transporting
P02647	Apolipoprotein A-I	2.78	Secreted	Metabolism
P21980	Protein-glutamine γ-glutamyltransferase 2	2.75	Secreted	Metabolism
P00738	Haptoglobin	2.56	Secreted	Binding
P07384	Calpain-1 catalytic subunit	2.54	Secreted	Metabolism
Q16378	Proline-rich protein 4	2.54	Nucleus	Metabolism
P11021	78 kDa glucose-regulated protein	2.51	Nucleus	Proliferation/differentiation
P62258	14-3-3 protein epsilon	2.44	Secreted	Metabolism
P01011	α-1-antichymotrypsin	2.40	Secreted	Immunity
P60174	Triosephosphate isomerase	2.27	NA	Immunity
P01871	Ig μ chain C region	2.23	Secreted	Immunity
Q14624	Inter-α-trypsin inhibitor heavy chain H4	2.19	Secreted	Metabolism
P00751	Complement factor B	2.07	Secreted	Immunity
P14625	Endoplasmin	2.07	Secreted	Apoptosis
Q13421	Mesothelin	2.07	Mitochondrion	Metabolism

Abbreviations: LOI, lovastatin insensitive; NA, no annotation.

Verification of proteins identified in tear fluid samples by Western blot analysis

The images from MS/MS spectra of Annexin A1 and Apo A-I identified by LC-MS/MS are shown in Figure 3A and B. These two proteins were chosen to verify the observed changes by Western blotting. After treatment, Annexin A1 was downregulated and ApoA1 was upregulated in both groups, consistent with the proteomic results (Figure 3C).

Figure 3

Proteins identified by MS/MS and Western blot analysis.

Notes: (A) MS/MS spectrum of peptide DITSDTSGDFRNALLSLAK from Annexin A1; (B) MS/MS spectrum of peptide DLATVYVDVLK from ApoA-1; and (C) Western blot analysis of Annexin A1 and ApoA-1 in tear fluid before and after treatment in both groups. AC + AT group, acupuncture plus artificial tears; AT group, artificial tears only group.

Abbreviation: MS/MS, tandem mass spectrometry.

Discussion

In recent studies, acupuncture therapy was determined to be effective for dry eye patients and was shown to be partially better compared with artificial tear treatment.10 Specifically, acupuncture relieved the symptoms and increased watery secretion.11 Our study validated these conclusions. In addition, we compared AC + AT treatment with artificial tear therapy alone. OSDI scores and symptoms were significantly improved in the AT + AC group compared to the AT group, indicating that acupuncture has a subjective and comprehensive beneficial effect on dry eye. One possible reason for this observation is that acupuncture can influence synthesis and secretion by the lacrimal gland. Others have postulated that acupuncture may reduce tension and alleviate pain intensity.12 Regardless, the mechanisms need to be confirmed. Acupuncture is reportedly associated with a significant increase in the secretion of serum estradiol as well as a reduction in the secretion of serum follicle-stimulating hormone and luteinizing hormone.13 However, an interesting phenomenon observed in this study was that the levels of these hormones remained the same. One possible reason for this could be that all the acupoints used in this study are located near the eye and are not gynecological acupoints.

Tear proteins have an important role in the maintenance of the ocular surface, and changes in the quality and quantity of tear components reflect changes in the health of the ocular surface. We successfully identified 2,411 proteins, among which 142 proteins were downregulated (ie, Annexin A1, myosin-14, neuroblast differentiation-associated protein AHNAK, leukocyte elastase inhibitor, and protein S100-A9) and 169 proteins were upregulated (ie, Apo A-I, complement C3, hemopexin, retinal dehydrogenase 1, clusterin, and ceruloplasmin).

Among the downregulated proteins, 44.37% are located in the cytoplasm; 28.99% of the upregulated proteins are secreted. This suggests that after treatment, more proteins are secreted into the tear fluid from the intracellular space. The pathogenesis of dry eye was traditionally ascribed to a decrease in tear production and decreased tear stability. As the mucous layer is composed of secretory, gel-forming, and transmembrane ocular surface mucus to stabilize the tear film,14 the observed upregulation of secreted proteins suggests increased production and tear stability.

The constituent ratio of protein function indicates that immunity-related proteins were upregulated after treatment and that those involved in apoptosis were downregulated. Dry eye has many causes, including inflammation and apoptosis, and anti-inflammation and ocular surface repair have proven to be useful in treating this condition.15 Proteins involved in transport, signal transduction, and regulation were found to be upregulated, and cell components and proliferation-related proteins were relatively downregulated. This interesting phenomenon suggests that acupuncture and artificial tear treatment may increase protein synthesis. Although the exact mechanisms of acupuncture are currently unknown, it is likely that the nervous system, neurotransmitters, and endogenous substances are involved in needle stimulation.16

Annexin A1, an endogenous anti-inflammatory molecule described as a repressor of the innate immune response,17 is a calcium-binding protein that promotes phagocyte migration and infiltration of granulocytes at wound sites and acts as an antimicrobial agent.18 Annexin A1 is upregulated under pathological conditions, such as in multiple sclerosis and hypoxic-ischemic brain damage. In addition, Annexin A1 protects against N-methyl-D-aspartate-induced brain damage, and Annexins I and V exert neurotrophic effects on cultured neurons.19 Thus, downregulated Annexin A1 after treatment indicated improvement in pathological conditions. S100-A9 is an inflammation-associated protein mainly expressed in granulocytes and epithelial cells; it is upregulated in tears of human dry eye patients and is associated with the severity of symptoms.20 A100-A9 is also upregulated in Sjögren’s syndrome, which is associated with dry eye and induces autoimmune dacryoadenitis in a rabbit model.21 As a first-line vertebrate immune defense, the polymeric immunoglobulin receptor transports polymeric IgA and IgM across the epithelium to mucosal secretions, whereby the cleaved ectodomain becomes a component of secretory antibodies or when the unbound ligand form binds and excludes bacteria.22 The fact that inflammation-associated proteins were downregulated after treatment indicates that a regional inhibitory inflammatory reaction occurred. One assumption that can be drawn from this is that the observed downregulated inflammatory proteins were induced by the stimulation of acupuncture, decreasing the release of inflammatory cytokines and the severity of dry eye.

The major apoprotein of high-density lipoprotein, Apo A-I is classically described as being synthesized only by the liver and the intestine. However, Apo A-I was recently found in the vitreous fluid and human RPE cells.23 Apo A-I has a protective effect on the corneal epithelium and may improve the epithelial conditions of the ocular surface.24 Clusterin is also present in human tears. It has been demonstrated that clusterin prevents and ameliorates ocular surface barrier disruption via a remarkable sealing mechanism that is dependent on the attainment of a critical all-or-none concentration in the tears: when the clusterin level drops below the critical all-or-none threshold, the barrier becomes vulnerable to desiccating stress.25 Clusterin indirectly enhances the colony-forming efficacy of corneal and limbal epithelial cells, suggesting its role in the epithelia–mesenchymal interaction.26 Serotransferrin is an iron-binding monomeric glycoprotein belonging to the innate immune system, and a significant decrease in transferrin in the tears of patients with early dry eye has been reported.27 These upregulated proteins observed after treatment may thus result in improvements in the ocular surface.

This study is an initial observation on the effects of acupuncture treatment on the clinical signs and tear composition of postmenopausal women with dry eye.

Limitations

The limitation of this study is its small sample size; indeed, results based on a larger sample size may be more convincing. In addition, the acupuncture course in this study was only 2 months, and we believe that a longer acupuncture course may have more obvious effects.

Conclusion

The purpose of this study was to investigate the clinical signs and changes in tear proteins after acupuncture among postmenopausal women. In the present study, AC + AT treatment increased protein synthesis and secretion and improved clinical symptoms. These results indicate that acupuncture may be a complementary therapy for postmenopausal dry eye.