Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 7
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

Introduction: Uterine leiomyoma is the most widespread benign tumor affecting women of childbearing age. There are still gaps in the understanding of its pathogenesiss. Telocytes are unique cells described in greater than 50 different locations inside the human body. The functional relationship of cells could clarify the pathogenesis of leiomyomata. In the current study, we focused on the identification of telocytes in all regions of the human uterus to explain their involvement in leiomyoma development.

Materials and Methods: Tissue samples from a healthy and myomatous uterus were stained for c-kit, tryptase, CD34 and PDGFRα to identify telocytes. Routine histology was performed to analyze tissue morphology and collagen deposits.

Results: Telocytes were detected in the cervix, corpus of the uterus and leiomyoma. The density of telocytes in fibroid foci was reduced compared with normal myometrium.

Conclusions: Our results demonstrated the existence of telocytes in all parts of the human body affected and unaff ected by leiomyoma of the uterus. In addition, telocytes were also present in leiomyoma foci. Our results suggest that the reduced density of telocytes is important for the pathomechanisms of myometrial growth, demonstrating its value as a main component of the myomatous architecture.

Go to article

Authors and Affiliations

Veronika Aleksandrovych
Magdalena Białas
Artur Pasternak
Tomasz Bereza
Marek Sajewicz
Jerzy Walocha
Krzysztof Gil
Download PDF Download RIS Download Bibtex

Abstract

Telocyte (TC) is an interstitial cell type with a small cellular body and extremely long tentacle-like extensions. TCs were discovered a decade ago and have specific morphological characteristics, immunohistochemical and secretome profi les, electrophysiological properties, microRNA expression. Moreover, they are different in gene expression from other cells. TCs play an important role in plenty of processes. Apparently, they are involved in homeostasis, remodelling, regeneration, repair, embryogenesis, angiogenesis and even tumorigenesis. “Telocytes need the world”, was emphasized by Professor Popescu and it will be actual at any time. This review summarizes particular features of TCs in different organs and systems, emphasizing their involvement in physiological and pathophysiological processes.

Go to article

Authors and Affiliations

Veronika Aleksandrovych
Artur Pasternak
Paweł Basta
Marek Sajewicz
Jerzy A. Walocha
Krzysztof Gil
Download PDF Download RIS Download Bibtex

Abstract

Background: The histology of the lung includes a variety of cell types. Fibrosis is a universal process, occurring in the skin, intestine, heart, muscles, kidney, blood vessels, liver, and also the lungs. Telocytes are a type of cells with a wide range of properties, which were previously described in healthy and disease-affected organs of human and animal organisms.

Aim: This study aimed to identify telocytes in the lungs of rats and discuss their possible role in the development of pulmonary fibrosis.

Methods: Tissue samples were taken from a group of ten male Wistar rats. Further histological and immunohistochemical analysis was performed. Double immunolabeling for c-kit, vimentin, CD34, and PDGFRα has revealed telocytes in the lungs.

Results: In all tissue samples, telocytes have been identified (in the area of interalveolar septa, close to blood vessels, and between the airway epithelium).

Conclusion: Telocytes might be directly and indirectly (through contact with stem cells, secretomes, and reduction in number) involved in the development of pulmonary fibrosis. The heterogeneity of the telocyte population in different pathologies and their subtypes, as well as their tendency to be common stress their important role in pathological physiology.
Go to article

Bibliography

1. Schraufnagel D.E.: Electron microscopy of the lung. New York: Marcel Dekker, CRC Press; 1990.
2. Hogan B., Tata P.R.: Cellular organization and biology of the respiratory system. Nat Cell Biol. 2019. https://doi.org/10.1038/s41556-019-0357-7.
3. Evren E., Ringqvist E., Willinger T.: Origin and ontogeny of lung macrophages: from mice to humans. Immunology. 2020; 160 (2): 126–138.
4. Awad M., Gaber W., Ibrahim D.: Onset of Appearance and Potential Significance of Telocytes in the Developing Fetal Lung. Microsc Microanal. 2019; 25 (5): 1246–1256.
5. Popescu L.M., Gherghiceanu M., Suciu L.C., Manole C.G., Hinescu M.E.: Telocytes and putative stem cells in the lungs: electron microscopy, electron tomography and laser scanning microscopy. Cell Tissue Res. 2011; 345 (3): 391–403.
6. Aleksandrovych V., Pasternak A., Basta P., Sajewicz M., Walocha J.A., Gil K.: Telocytes: facts, speculations and myths (Review article). Folia Med Cracov. 2017; 57 (1): 5–22.
7. Zheng Y., Li H., Manole C.G., Sun A., Ge J., Wang X.: Telocytes in trachea and lungs. J Cell Mol Med. 2011; 15: 2262–2268.
8. Aleksandrovych V., Walocha J.A., Gil K.: Telocytes in female reproductive system (human and animal). J Cell Mol Med. 2016; 20 (6): 994–1000.
9. Díaz-Flores L., Gutiérrez R., Díaz-Flores L.J.R., Goméz M.G., Sáez F.J., Madrid J.F.: Behaviour of telocytes during physiopathological activation. Semin Cell Dev Biol. 2016; 55: 50–61.
10. Hussein M.M., Mokhtar D.M.: The roles of telocytes in lung development and angiogenesis: An immunohistochemical, ultrastructural, scanning electron microscopy and morphometrical study. Dev Biol. 2018; 443 (2): 137–152.
11. Popescu L.M., Faussone-Pellegrini M.S.: TELOCYTES — a case of serendipity: the winding way from interstitial cells of Cajal (ICC), via interstitial Cajal-like cells (ICLC) to TELOCYTES. J Cell Mol Med. 2010; 14: 729–740.
12. Ibba-Manneschi L., Rosa I., Manetti M.: Telocyte implications in human pathology: An overview. Biol. 2016; 55: 62–69.
13. Liao Z., Chen Y., Duan C., Zhu K., Huang R., Zhao H., et al.: Cardiac telocytes inhibit cardiac microvascular endothelial cell apoptosis through exosomal miRNA-21-5p-targeted cdip1 silencing to improve angiogenesis following myocardial infarction. Theranostics. 2021; 11 (1): 268–291.
14. Zhaofu L., Dongqing C.: Cardiac Telocytes in Regeneration of Myocardium After Myocardial Infarction. Adv Exp Med Biol. 2016; 913: 229–239.
15. Milia A.F., Ruffo M., Manetti M., Rosa I., Conte D., Fazi M., et al.: Telocytes in Crohn’s disease. Cell Mol Med. 2013; 17 (12): 1525–1536.
16. Ibba-Manneschi L., Rosa I., Manetti M.: Telocytes in Chronic Inflammatory and Fibrotic Diseases. Adv Exp Med Biol. 2016; 913: 51–76.
17. Wolnicki M., Aleksandrovych V., Gil A., Pasternak A., Gil K.: Relation between ureteral telocytes and the hydronephrosis development in children. Folia Med Cracov. 2019; 59 (3): 31–44.
18. Aleksandrovych V., Pasternak A., Gil K.: Telocytes in the architecture of uterine fibroids. Folia Med Cracov. 2019; 59 (4): 33–44.
19. Aleksandrovych V., Białas M., Pasternak A., Bereza T., Sajewicz M., Walocha J., et al.: Identification of uterine telocytes and their architecture in leiomyoma. Folia Med Cracov. 2018; 58 (3): 89–102.
20. Manole C.G., Gherghiceanu M., Simionescu O.J.: Telocyte dynamics in psoriasis. Cell Mol Med. 2015; 19 (7): 1504–1519.
21. Jin L., Wang Z., Qi X.: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia: Case series and a review of the literature. Medicine (Baltimore). 2018; 97 (52): e13806.
22. Leuenberger P.: [Clinical importance of non-respiratory functions of the lung]. Schweiz Med Wochenschr. 1983; 113 (29): 1006–1010.
23. Wittmann J.: [Respiratory and non-respiratory functions of the lung]. Tierarztl Prax Suppl. 1987; 2: 33–36.
24. Aleksandrovych V., Kurnik-Łucka M., Bereza T., Białas M., Pasternak A., Cretoiu D., Walocha J.A., Gil K.: The Autonomic Innervation and Uterine Telocyte Interplay in Leiomyoma Formation. Cell Transplant. 2019; 28: 619–629.
25. Song D., Cretoiu D., Cretoiu S.M., Wang X.: Telocytes and lung disease. Histol Histopathol. 2016; 31 (12): 1303–1314.
26. Shi L., Dong N., Chen C., Wang X.: Potential roles of telocytes in lung diseases. Semin Cell Dev Biol. 2016; 55: 31–39.
27. Ciechanowicz A.: Stem Cells in Lungs. Adv Exp Med Biol. 2019; 1201: 261–274.
28. Rokicki W., Rokicki M., Wojtacha J., Dżeljijli A.: The role and importance of club cells (Clara cells) in the pathogenesis of some respiratory diseases. Kardiochir Torakochirurgia Pol. 2016; 13 (1): 26–30.
29. Ibba-Manneschi L., Rosa I., Manetti M.: Telocytes in Chronic Inflammatory and Fibrotic Diseases. Adv Exp Med Biol. 2016; 913: 51–76.
Go to article

Authors and Affiliations

Anna Gil
1
Veronika Aleksandrovych
1

  1. Department of Pathophysiology, Jagiellonian University Medical College, Kraków, Poland
Download PDF Download RIS Download Bibtex

Abstract

Background: Uterine leiomyoma is the most widespread benign tumor affecting women of childbearing age. There are still gaps in the understanding of its pathogenesis. Telocytes are unique cells found in more than 50 different locations inside the human body. The functional relationship between cells could clarify the pathogenesis of leiomyomata. Examination of membrane receptors on telocytes could explain their role in fibrosis, oxidative stress, and myometrial contractility.

Aim: This research was conducted to assess the density of telocytes in terms of their putative role in leiomyoma formation by focusing on their correlation with the expression of estrogen and progesterone receptors.

Methods: For gross evaluation of uterine tissue samples from leiomyoma, routine histology of adjacent and unaffected myometrium was performed. Immunohistochemical analysis of c-kit, tryptase, CD34, PDGFRα (telocyte-specific), and ER and PRs (estrogen and progesterone receptors) was performed to examine uterine telocytes and the expression of sex steroid receptors.

Results: The decline in telocyte density in leiomyoma foci was correlated with high progesterone expression and low estrogen receptor expression. The unchanged myometrium showed the opposite correlation and balance between both steroid hormone receptors. The difference in sex steroid receptor expression is correlated with the density of uterine telocytes, which emphasizes their conductor function.

Conclusions: A reduction in telocyte density and the changes in examined marker expression demon-strate the involvement of telocytes in local homeostasis. The expression of membrane receptors explicitly indicates their functional potential in the human myometrium, focusing attention on contractility and local homeostasis.

Go to article

Authors and Affiliations

Veronika Aleksandrovych
Anna Gil
Anna Wrona
Download PDF Download RIS Download Bibtex

Abstract

I n t r o d u c t i o n: Hydronephrosis is an actual pediatric problem, affecting children in the anteand neonatal periods. Intrinsic stenosis is due to external obstruction and creates a pathophysiological basis of this urological pathology. Co-localization of ureter with a renal vasculature also could not be omitted from this point of view. Mesenchymal cells, partially telocytes, are important for local fibrosis development and hydronephrosis formation as well. In the current study, we focused on identification of telocytes in the human ureters to hypothesize their role in hydronephrosis pathophysiology.

M a t e r i a l a n d Me t h o d s: The samples were taken from 18 surgically treated patients with hydronephrosis (due to ureteral obstruction and crossing renal vessel). The control group consisted of 10 patients suffered from a non-obstructive disease of the urinary tract — predominantly renal tumors. Tissue samples from a ureter were stained for c-kit, tryptase, CD34 and PDGFRα to identify telocytes. Routine histology was performed to analyze tissue morphology, collagen deposits and mast cell’s profile.

R e s u l t s: Telocytes were detected in the ureteral wall. In patients with hydronephrosis we revealed decreasing density of telocytes, the prevalence of collagen, rise in mast cells amount and the ureteral wall thickening. In ureters with crossing renal vessels as a primary etiologic factor more telocytes have been observed in comparison with the obstructive hydronephrosis.

C o n c l u s i o n s: A declined density of telocytes accompanied hydronephrosis development. Increased number of mast cells in the ureteral wall reflects a local inflammation, while detailed observation of collagen/muscle deposits and density of telocytes reveal a difference depended on etiologic factor (obstruction or crossing vessel) in patients with hydronephrosis.

Go to article

Authors and Affiliations

Michał Wolnicki
Veronika Aleksandrovych
Anna Gil
Artur Pasternak
Krzysztof Gil
Download PDF Download RIS Download Bibtex

Abstract

The adaptation response of myocardium angiogenesis stimulated by specific exercise intensities remains unclear. The aims of this study is to explore the effect of different intensities aerobic exercise to cardiac angiogenesis regulation via HIF-1α, PGC-1α, VEGF, and CD34+ in Wistar rats. Wistar rats were divided into control and exercise groups. Exercise groups were trained on a treadmill for 12 weeks, 30 min/day for 5 days with low, moderate, and high-intensity groups. The rats were sacrificed, and the myocardium was collected and preserved at -80°C until used. Cardiac protein samples were extracted and run for Western blotting using the specific antibodies: hypoxia-inducible factor (HIF)-1α, Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α), vascular endothelial growth factor (VEGF), and Cluster of differentiation 34 (CD34+). Results showed that protein expression of HIF-1α, PGC-1α, VEGF, and CD34+ was increased significantly by different intensities in the exercise group compared to the control. A correlation statistics test showed that there was a strong correlation effect of HIF-1α on VEGF protein expression in low (p=0.047) and high intensity exercise groups (p=0.009), but no effect was found in the moderate groups. In addition, there was a significant strong effect of PGC-1α on VEGF protein expression in the moderate groups (p=0.037), but no effect was found in other groups. In conclusion, different exercise intensities induce a different modulation pattern of proteins which might be responsible for cardiac adaptation, especially angiogenesis.
Go to article

Bibliography

Allen TJ (2004) Textbook of Work Physiology: Physiological Bases of Exercise, Fourth Edition. Physiother. Canada.
American Psychological Association (2007) Chapter 3. Exercise Protocols Using Rats and Mice. In: Resource book for the design of animal exercise protocols.
Arany Z, Foo SY, Ma Y, Ruas JL, Bommi-Reddy A, Girnun G, Cooper M, Laznik D, Chinsomboon J, Rangwala SM, Baek KH, Rosenzweig A, Spiegelman BM (2008) HIF-independent regulation of VEGF and angiogenesis by the transcriptional coactivator PGC-1alpha. Nature 451(7181): 1008-12.
BioRad (2016) General Protocol for Western Blotting. Boletín 6376.
Broxterman RM, Layec G, Hureau TJ, Amann M, Richardson RS (2017) Skeletal Muscle Bioenergetics During All-Out Exercise: Mechanistic Insight Into The Oxygen Uptake Slow Component And Neuromuscular Fatigue. J Appl Physiol 122(5): 1208-1217.
Chinsomboon J, Ruas J, Gupta RK, Thom R, Shoag J, Rowe GC, Sawada N, Raghuram S, Arany Z (2009) The transcriptional coactivator PGC-1alpha mediates exercise- -induced angiogenesis in skeletal muscle. Proc Natl Acad Sci U S A 106(50): 21401-6.
Davies KJ (2016) Adaptive homeostasisMol Aspects Med 49: 1-7. Di Meo, S, Napolitano, G, Venditti, P (2019) Mediators of Physical Activity Protection against ROS-Linked Skeletal Muscle Damage. International journal of molecular sciences 20(12): 3024.
Golbidi S, Laher I (2012) Exercise and the cardiovascular system. Cardiol Res Pract 2012: 210852.
Gunadi JW, Tarawan VM, Daniel Ray HR, Wahyudianingsih R, Lucretia T, Tanuwijaya F, Lesmana R, Supratman U, Setiawan I (2020) Different training intensities induced autophagy and histopathology appearances potentially associated with lipid metabolism in wistar rat liver. Heliyon 6(5): e03874.
Hoppeler H, Vogt M (2001) Muscle tissue adaptations to hypoxia. J Exp Biol 204(Pt 18): 3133-9.
Jensen EC. The Basics of Western Blotting (2012) Anat Rec (Hoboken) 295(3): 369-71.
Jones, JH (2007) Resource Book for the Design of Animal Exercise Protocols, American Journal of Veterinary Research 68(6): 583-583.
Kang C, O’Moore KM, Dickman JR, Ji LL (2009) Exercise Activation Of Muscle Peroxisome Proliferator-Activated Receptor-Gamma Coactivator-1alpha Signaling Is Redox Sensitive. Free Radic Biol Med 47(10): 1394-400.
Koutroumpi M, Dimopoulos S, Psarra K, Kyprianou T, Nanas, S (2012) Circulating Endothelial And Progenitor Cells: Evidence From Acute And Long-Term Exercise Effects. World Journal Of Cardiology 4(12): 312-326.
Korivi, M, Hou, CW, Chen, CY, Lee, JP, Kesireddy, SR, Kuo, CH (2010) Angiogenesis: Role of Exercise Training and Aging. Adapt Med 2(1): 29-41.
Kremelberg, D (2011) Pearson’s r, Chi-square, T-Test, and ANOVA. In: Practical statistics: A quick and easy guide to IBM® SPSS® statistics, STATA, and other statistical software. SAGE Publications, Inc, pp: 119-204).
Kutikhin AG, Sinitsky MY, Yuzhalin AE, Velikanova EA. Shear stress: An essential driver of endothelial progenitor cells (2018) J Mol Cell Cardiol 118: 46-69.
Laboratory Animal Anaesthesia. In: Laboratory Animal Anaesthesia (2009) 13ed ed. Lansford KA, Shill DD, Dicks AB, Marshburn MP, Southern WM, Jenkins NT. Effect Of Acute Exercise on Circulating Angiogenic Cell and Microparticle Populations (2016) Exp Physiol 101(1):155-67.
Larsen FJ, Schiffer TA, Ørtenblad N, Zinner C, Morales- -Alamo D, Willis SJ, Calbet JA, Holmberg HC, Boushel R (2016) High-intensity sprint training inhibits mitochondrial respiration through aconitase inactivation. FASEB J 1: 417-27.
Laufs U, Werner N, Link A, Endres M, Wassmann S, Jürgens K, Miche E, Böhm M, Nickenig G (2004) Physical Training Increases Endothelial Progenitor Cells, Inhibits Neointima Formation, and Enhances Angiogenesis. Circulation 109(2): 220-6.
Lesmana R, Iwasaki T, Iizuka Y, Amano I, Shimokawa N, Koibuchi N (2016) The Change in Thyroid Hormone Signaling by Altered Training Intensity in Male Rat Skeletal Muscle. Endocr J 63(8):727-38.
Li L, Liu H, Xu C, Deng M, Song M, Yu X, Xu S, Zhao X (2017) VEGF promotes endothelial progenitor cell differentiation and vascular repair through connexin 43. Stem Cell Res Ther 8(1): 237.
Lian X, Bao X, Al-Ahmad A, Liu J, Wu Y, Dong W, Dunn KK, Shusta EV, Palecek, S. P (2014) Efficient differentiation of human pluripotent stem cells to endothelial progenitors via small-molecule activation of WNT signaling. Stem cell reports 3(5): 804-816.
Lindholm ME, Fischer H, Poellinger L, Johnson RS, Gustafsson, T, Sundberg CJ, Rundqvist H (2014) Negative Regulation of HIF in Skeletal Muscle of Elite Endurance Athletes: A Tentative Mechanism Promoting Oxidative Metabolism. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 307(3): R248-R255.
Lindholm ME, Rundqvist H (2016) Skeletal Muscle Hypoxia-Inducible Factor-1 and Exercise. Experimental Physiology 101(1): 28-32.
Mac Gabhann F, Ji JW, and Popel AS (2007) VEGF gradients, receptor activation, and sprout guidance in resting and exercising skeletal muscle. J. Appl. Physiol 102: 722-734
Mason, SA, Morrison D, McConell, GK, Wadley, GD (2016) Muscle Redox Signalling Pathways In Exercise. Role of Antioxidants. Free Radical Biology & Medicine 98: 29-45.
Mrakic-Sposta S, Gussoni M, Porcelli S, Pugliese L, Pavei G, Bellistri G, Montorsi M, Tacchini, P, Vezzoli A (2015) Training Effects On ROS Production Determined by Electron Paramagnetic Resonance in Master Swimmers. Oxidative Medicine and Cellular Longevity 2015 804794.
Niecknig H, Tug S, Reyes BD, Kirsch M, Fandrey J, Berchner-Pfannschmidt U (2012) Role of Reactive Oxygen Species in The Regulation of HIF-1 by Prolyl Hydroxylase 2 Under Mild Hypoxia. Free Radical Research 46(6): 705-717.
National Research Council (US) Committee for the update of the guide for the care and use of laboratory animals (2011) Guide for the Care and Use of Laboratory Animals. 8th ed., Washington (DC): National Academies Press (US).
Ohno H, Shirato K, Sakurai T, Ogasawara J, Sumitani Y, Sato S, Imaizumi K, Ishida H, Kizaki T (2012) Effect of exercise on HIF-1 and VEGF signaling. J. Phys. Fit. Sport 1(1): 5-16.
Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C, Catapano AL et al (2016) 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Eur Heart J 37(29): 2315-2381.
Radak Z, Zhao Z, Koltai E, Ohno H, Atalay M (2013) Oxygen Consumption and Usage During Physical Exercise: The Balance Between Oxidative Stress and ROS-Dependent Adaptive Signaling. Antioxid Redox Signal. 18(10): 1208-46.
Recchioni R, Marcheselli F, Antonicelli R, Lazzarini R, Mensà E, Testa R, Procopio AD, Olivieri F (2016) Physical Activity and Progenitor Cell-Mediated Endothelial Repair in Chronic Heart Failure: Is There A Role For Epigenetics? Mech Ageing Dev 159: 71-80.
Roh HT, Cho SY, Yoon HG, So WY(2017) Effect Of Exercise Intensity On Neurotrophic Factors and Blood-Brain Barrier Permeability Induced by Oxidative-Nitrosative Stress in Male College Students. Int J Sport Nutr Exerc Metab 27(3): 239-246.
Rowe, GC, Jang C, Patten IS, Arany Z (2011) PGC-1β regulates angiogenesis in skeletal muscle. American journal of physiology. Endocrinology and metabolism 301(1): E155-E163.
Scarpulla RC, Vega RB, Kelly DP (2012) Transcriptional integration of mitochondrial biogenesis. Trends in endocrinology and metabolism: TEM 23(9): 459-466.
Semenza GL (2011) Hypoxia-Inducible Factor 1: Regulator of Mitochondrial Metabolism and Mediator of Ischemic Preconditioning. Biochimica et Biophysica Acta 1813(7): 1263-1268.
Serocki M, Bartoszewska S, Janaszak-Jasiecka A, Ochocka RJ, Collawn JF, Bartoszewski R (2018) miRNAs Regulate the HIF Switch During Hypoxia: A Novel Therapeutic Target. Angiogenesis 21(2): 183-202.
Shibuya M (2011) Vascular Endothelial Growth Factor (VEGF) and Its Receptor (VEGFR) Signaling in Angiogenesis: A Crucial Target for Anti- and Pro-Angiogenic Therapies. Genes & cancer 2(12): 1097-1105.
Sylviana N, Helja N, Qolbi H H, Goenawan H, Lesmana R (2018) Effect of Swimming Exercise to Cardiac PGC-1α and HIF-1α Gene Expression in Mice. Asian J Sports Med 9(4): e65079.
Tang XY, Hong HS, Chen LL, Lin XH, Lin JH, Lin Z (2011) Effects Of Exercise Of Different Intensities on The Angiogenesis, Infarct Healing, and Function of The Left Ventricle in Postmyocardial Infarction Rats. Coronary Artery Disease 22(7): 497-506.
Thijssen DH, Torella D, Hopman MT, Ellison GM (2009) The Role of Endothelial Progenitor and Cardiac Stem Cells in The Cardiovascular Adaptations to Age and Exercise. Frontiers in bioscience (Landmark edition) 14: 4685-4702.
Volaklis KA, Tokmakidis, SP, Halle, M (2013) Acute and Chronic Effects of Exercise on Circulating Endothelial Progenitor Cells in Healthy and Diseased Patients. Clinical Research In Cardiology : Official Journal Of The German Cardiac Society 102(4): 249-257.
Weeks KL, McMullen JR (2011) The athlete’s heart vs the failing heart: can signaling explain the two distinct outcomes? Physiology (Bethesda, Md.) 26(2): 97-105.
Wenz T (2013) Regulation of Mitochondrial Biogenesis and PGC-1α Under Cellular Stress. Mitochondrion 13(2): 134-142.
Wilson MG, Ellison, GM, Cable, NT (2016) Basic Science Behind The Cardiovascular Benefits of Exercise. British Journal of Sports Medicine 50(2): 93-99.
Zokaei A, Javid, NM (2017) Report of Health Care The Effect of Eight Weeks of High-Intensity Interval Training on Genes Expression of eNOS, HIF-1 and VEGF in Myocardial Infarction Rats 3(4): 31-37.
Go to article

Authors and Affiliations

N. Sylviana
1 2
H. Goenawan
1 2
Y. Susanti
1 2
R. Lesmana
1 2
I. Megantara
1 2
Setiawan
1

  1. Physiology Division, Biomedical Sciences Department Faculty Medicine, Universitas Padjadjaran, Jatinangor, Jawa Barat, Indonesia
  2. Physiology Molecular Laboratory, Biological Activity Division, Central Laboratories, Universitas Padjadjaran, Jatinangor, Jawa Barat, Indonesia
Download PDF Download RIS Download Bibtex

Abstract

Knowledge of uterine fibroids has existed since the time of Hippocrates. However, there are still wide gaps in the understanding of its pathogenesis. No single theory explains the background of uterine fibroid pathology, which affects more than 50% of women worldwide. By contrast, a newly depicted cell type called telocytes was only recently identified in the past twenty years. Th ese cells have evoked ambivalent opinions in the scientific community. The unique features of telocytes coupled with experimental evidence by numerous researchers and our hypotheses and conceptions are discussed in this review. We emphasize the main telocyte interactions in the context of the uterine fibroid architecture. This review reveals the pivotal role of telocytes, describing their contacts with smooth muscle cells, fibroblasts, vessels and nerves, inflammatory cells and stem cells. Our data are based on the latest publications and our own results.

Go to article

Authors and Affiliations

Veronika Aleksandrovych
Artur Pasternak
Krzysztof Gil

This page uses 'cookies'. Learn more