Introduction
A gland is a functional unit of cells that works together to create and release a product into a duct or the bloodstream. Two principal types of glands exist: exocrine and endocrine. The key difference between the 2 types is that exocrine glands secrete substances into a ductal system to an epithelial surface, whereas endocrine glands secrete products directly into the bloodstream.[1] Exocrine secretions form in the acinus, a small cluster of cells at the origination of glandular ducts. Exocrine glands subclassify into subtypes based on the method of secretion, the compound produced, or the shape of the gland.
Issues of Concern
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Issues of Concern
This topic will address:
- Various cell types found within the exocrine gland and their functions
- Embryologic development of exocrine glands
- Organ systems impacted by exocrine physiology
- Functions of exocrine glands
- Related clinical testing
- Pathophysiology of exocrine glands
- Significant clinical aspects
Cellular Level
Exocrine Glands
Exocrine glands are comprised of an acinus and a duct with different cell types, respectively. They are found in many organs within the body and contain a wide range of cell types, demonstrating a wide variety of functions of their secretions.
While the duct functions primarily to transport glandular secretions, the acinus is responsible for producing glandular secretions and, as such, shows more variety in cellular composition. Typical cell types within the acinus include serous, mucinous, or sebaceous.
- Serous cells: Secrete an isotonic fluid that contains proteins such as enzymes; salivary glands are made up of serous cells to a large extent.[2]
- Mucinous glands: Secrete mucus; a typical example is the Brunner glands in the duodenum.
- Sebaceous glands: Secrete sebum, an oily compound; sebaceous glands are most prevalent in the face, scalp, groin, and armpits.
Cell types can also be differentiated histologically. Mucous cells typically stain lighter than their serous counterparts when stained with hematoxylin and eosin.
Intralobular and Interlobar Ducts
As ducts move from the acinus toward the final target, secretions enter the intralobular duct. Intralobular ducts have a simple cuboidal epithelium commonly surrounded by parenchyma. Intralobular ducts drain into interlobular ducts, which are a simple columnar epithelium. The final ductal unit is the interlobar duct, recognized by a stratified columnar epithelium. Connective tissue surrounds both interlobular and interlobar ducts.
Development
The initial manifestation of exocrine gland formation is epithelial budding resulting from a complex interaction between mesenchymal and epithelial cell populations.[3] This initial ingrowth period is influenced by fibroblast growth factors, most notably FGF10 and cadherin-2.[4] Other transcription factors that have been shown to contribute to epithelial budding include HlxB9, Isl1, LEF-1, Msx1/2, Pbx1, Pdx1, and Tbx3.[5]
Following the initial formation of the epithelial bud, ductal elongation occurs. This process undergoes mediation by a large group of molecular signals such as Netrin-1, TIMP1, amphiregulin, IGF1, and leukemia inhibitory factors.[5] Several matrix metalloproteinases (MMPs) assist basement membrane renewal and facilitate ductal elongation.[6][7] After an initial period of ductal elongation, the exocrine gland begins to form ductal branches. NF-kappa-B is thought to play a role,[8] as well as sonic hedgehog and Wnts.[3] As the duct begins to elongate, the acinus undergoes a period of cell proliferation and differentiation. Due to the large variety in exocrine gland function, the exact number of cellular signals and interactions is immense. In general, however, cell adhesion molecules such as laminin and cadherins play a large role.[9]
Exocrine morphogenesis is a rapid process. Ductal elongation and branching typically occur in less than a week, with acini formation occurring 5 to 9 days later.[10][11] In a relatively short developmental period, exocrine glands form and can begin secreting a functional product.
Organ Systems Involved
Due to the diverse number and function of epithelial surfaces in the body, many organ systems utilize exocrine glands to carry out their respective actions.
Skin
The skin has a variety of exocrine glands, including eccrine sweat glands and sebaceous glands. Eccrine sweat glands are the most widespread sweat glands in the body and are present on nearly every external body surface. The sweat produced is clear with little to no oil, in contrast to sebaceous glands, also found on the skin, which secrete the more oily substance sebum.
Salivary Glands
The salivary glands in the mouth are another example of exocrine glands, including the parotid, submandibular, and sublingual glands. While each gland has a unique mixture of serous and mucous cells, together, the salivary glands act to begin the process of food digestion while also lubricating and protecting the mucosal surfaces.
Stomach
The stomach contains multiple exocrine glands, including the pyloric, cardiac, and fundic glands. These glands incorporate many different cell types, including the parietal, chief, and G. Together, they regulate the gastric pH, release enzymes to break down food products into a digestible form and assist with absorbing necessary vitamins and minerals.
Pancreas
The pancreas has both an endocrine and an exocrine function. The exocrine pancreas assists in food digestion by releasing a secretion rich in bicarbonate, which helps to neutralize the acidic environment created in the stomach. The secretion also includes digestive enzymes.
Duodenum
Brunner glands are present in the duodenum of the small intestine. These exocrine glands are submucosal and produce a mucous product that protects the duodenum from stomach acid. The alkaline nature of the secretion also activates intestinal enzymes to assist with food breakdown and absorption.
Breast
The mammary gland is one of the most well-known examples of an exocrine gland found in the breast. It produces nutrient-rich milk, providing passive immunity to a baby’s immune system.
Function
The specific function of exocrine glands within the body varies by location and organ system. However, the primary role is to create a secretion that subsequently gets released through a ductal system onto an epithelial surface. Examples include secretions that assist in food digestion, mucosal protection, thermoregulation, lubrication, and nutrition.
Mechanism
The 3 mechanisms by which exocrine glands release their secretions include merocrine, apocrine, and holocrine.
- Merocrine glands: The most common subtype, merocrine gland secretions exit the cell via exocytosis. This method of secretion does not damage the cell. An example of merocrine secretion is the eccrine sweat gland.
- Apocrine glands: These form buds of the membrane that break off into the duct, losing part of the cellular membrane in the process. A well-known apocrine gland is the breastmilk-producing mammary gland.
- Holocrine glands: The cellular membrane of holocrine glands ruptures to release its product into the duct. Sebaceous glands represent holocrine secretion.
Related Testing
In general, testing for an individual exocrine gland function is not performed. However, dysfunction of exocrine glands can create a wide range of clinical manifestations. Imaging may be performed to confirm a diagnosis of blocked glands. Sialolithiasis refers to instances where a stone becomes lodged within the salivary gland or duct, and sialoadenitis refers to inflammation of the gland. CT and ultrasound are effective methods of identifying and localizing stones.[12]
The liver acts as an exocrine gland when creating and excreting bile to be stored in the gallbladder, awaiting expulsion and release through the pancreatic duct into the duodenum. Obstruction, at any point in this pathway, can cause cholecystitis due to inflammation and dysfunction of the gallbladder. Ultrasound is the initial diagnostic test to diagnose cholecystitis.[13]
In cystic fibrosis, sodium and chloride are not reabsorbed within the sweat duct due to a dysfunctional cystic fibrosis transmembrane conductance regulator (CFTR) protein, resulting in abnormally salty skin. The sweat chloride test is the primary test for diagnosing cystic fibrosis.[14]
Pancreatic insufficiency occurs when the exocrine glands of the pancreas can no longer produce the digestive enzymes necessary for food breakdown in the small intestine. Common etiologies include chronic pancreatitis, cystic fibrosis, and hereditary hemochromatosis. Several methods can be used to evaluate the function of the exocrine pancreas. Fat malabsorption can lead to deficiencies in fat-soluble vitamins A, D, E, and K. Thus, vitamin levels can be used to estimate pancreatic function.[15] Fecal elastase-1 testing is another method with relatively high specificity and sensitivity. Low levels of fecal elastase-1 indicate a poorly functioning exocrine pancreas.[16] However, the most sensitive diagnostic method for exocrine pancreatic insufficiency is direct pancreatic function tests such as the cholecystokinin (CCK) or secretin stimulation test.[17]
Pathophysiology
Sjögren Syndrome
Sjögren syndrome is commonly associated with rheumatoid arthritis and other rheumatic diseases. The syndrome is an autoimmune disorder that demonstrates decreased lacrimal and salivary gland function that can also have associated systemic symptoms.[18][19] The disease is characterized by eye and mouth dryness due to the gland dysfunction. Due to mouth dryness, patients with Sjogren syndrome show increased rates of oral candidiasis and dental caries.[18][20]
Cystic Fibrosis
Cystic fibrosis is an autosomal recessive disease that causes impaired chloride transport due to a mutation of the CFTR protein. Because CFTR is involved in the production of sweat, mucus, and digestive fluids, the mutation causes a direct effect on exocrine gland secretions. Indeed, approximately 90% of infants born with cystic fibrosis will develop pancreatic insufficiency by one year of age.[21]
Acne vulgaris
The prevalence of acne is an estimated 35% to 90% in adolescents.[22] The disorder affects the pilosebaceous unit, of which sebaceous glands are an example. The pathogenesis is multifactorial and often involves hyperkeratinization of the follicle, increased sebum production, and proliferation of Propionibacterium acnes with associated inflammation. As sebum accumulates, an open comedo forms, also known as a white head. Hyperkeratinization and increased sebum production lead to clogging of the pores of the pilosebaceous unit. As the lipids within the sebum oxidize, the follicular orifice opens, forming an open comedo, or blackhead.
Acne treatment largely depends on the severity of inflammatory symptoms, but topical retinoids are usually the first-line treatment, although antimicrobial agents are an additional option for refractory cases.[23] for severe cases of nodulocystic acne or patients who have failed treatment with systemic antibiotics, oral isotretinoin is the therapeutic choice.[24]
Clinical Significance
Because the exocrine gland can be found in many organs and serves a wide variety of functions within the body, an understanding of the physiology of exocrine glands is essential for healthcare workers. Exocrine glands play a key role in the physiology of many organ systems, from the skin to the pancreas, providing the body with a method to release secretions containing proteins, mucus, and other products to epithelial surfaces around the body. Owing to their varied and essential roles, the dysfunction of exocrine glands is associated with diseases as wide-ranging as acne vulgaris to Sjögren syndrome.
References
Murphrey MB, Safadi AO, Vaidya T. Histology, Apocrine Gland. StatPearls. 2024 Jan:(): [PubMed PMID: 29489220]
Holmberg KV,Hoffman MP, Anatomy, biogenesis and regeneration of salivary glands. Monographs in oral science. 2014 [PubMed PMID: 24862590]
Govindarajan V,Ito M,Makarenkova HP,Lang RA,Overbeek PA, Endogenous and ectopic gland induction by FGF-10. Developmental biology. 2000 Sep 1; [PubMed PMID: 10964474]
Level 3 (low-level) evidenceWang J, Laurie GW. Organogenesis of the exocrine gland. Developmental biology. 2004 Sep 1:273(1):1-22 [PubMed PMID: 15302594]
Level 3 (low-level) evidenceWitty JP,Wright JH,Matrisian LM, Matrix metalloproteinases are expressed during ductal and alveolar mammary morphogenesis, and misregulation of stromelysin-1 in transgenic mice induces unscheduled alveolar development. Molecular biology of the cell. 1995 Oct; [PubMed PMID: 8573787]
Level 3 (low-level) evidenceSympson CJ, Talhouk RS, Alexander CM, Chin JR, Clift SM, Bissell MJ, Werb Z. Targeted expression of stromelysin-1 in mammary gland provides evidence for a role of proteinases in branching morphogenesis and the requirement for an intact basement membrane for tissue-specific gene expression. The Journal of cell biology. 1994 May:125(3):681-93 [PubMed PMID: 8175886]
Level 3 (low-level) evidenceBrantley DM,Chen CL,Muraoka RS,Bushdid PB,Bradberry JL,Kittrell F,Medina D,Matrisian LM,Kerr LD,Yull FE, Nuclear factor-kappaB (NF-kappaB) regulates proliferation and branching in mouse mammary epithelium. Molecular biology of the cell. 2001 May; [PubMed PMID: 11359934]
Level 3 (low-level) evidenceYurchenco PD, Amenta PS, Patton BL. Basement membrane assembly, stability and activities observed through a developmental lens. Matrix biology : journal of the International Society for Matrix Biology. 2004 Jan:22(7):521-38 [PubMed PMID: 14996432]
Level 3 (low-level) evidenceWessells NK,Evans J, Ultrastructural studies of early morphogenesis and cytodifferentiation in the embryonic mammalian pancreas. Developmental biology. 1968 Apr; [PubMed PMID: 5650009]
Level 3 (low-level) evidenceWolff MS, Mirels L, Lagner J, Hand AR. Development of the rat sublingual gland: a light and electron microscopic immunocytochemical study. The Anatomical record. 2002 Jan 1:266(1):30-42 [PubMed PMID: 11748569]
Level 3 (low-level) evidenceThomas WW,Douglas JE,Rassekh CH, Accuracy of Ultrasonography and Computed Tomography in the Evaluation of Patients Undergoing Sialendoscopy for Sialolithiasis. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery. 2017 May; [PubMed PMID: 28457224]
Shea JA, Berlin JA, Escarce JJ, Clarke JR, Kinosian BP, Cabana MD, Tsai WW, Horangic N, Malet PF, Schwartz JS. Revised estimates of diagnostic test sensitivity and specificity in suspected biliary tract disease. Archives of internal medicine. 1994 Nov 28:154(22):2573-81 [PubMed PMID: 7979854]
Level 1 (high-level) evidenceDenning CR,Huang NN,Cuasay LR,Shwachman H,Tocci P,Warwick WJ,Gibson LE, Cooperative study comparing three methods of performing sweat tests to diagnose cystic fibrosis. Pediatrics. 1980 Nov; [PubMed PMID: 7432881]
Dutta SK, Bustin MP, Russell RM, Costa BS. Deficiency of fat-soluble vitamins in treated patients with pancreatic insufficiency. Annals of internal medicine. 1982 Oct:97(4):549-52 [PubMed PMID: 6922690]
Domínguez-Muñoz JE,Hieronymus C,Sauerbruch T,Malfertheiner P, Fecal elastase test: evaluation of a new noninvasive pancreatic function test. The American journal of gastroenterology. 1995 Oct; [PubMed PMID: 7572904]
Heij HA, Obertop H, Schmitz PI, van Blankenstein M, Westbroek DL. Evaluation of the secretin-cholecystokinin test for chronic pancreatitis by discriminant analysis. Scandinavian journal of gastroenterology. 1986 Jan:21(1):35-40 [PubMed PMID: 3952450]
Wu AJ, The oral component of Sjögren's syndrome: pass the scalpel and check the water. Current rheumatology reports. 2003 Aug; [PubMed PMID: 14531958]
Asmussen K, Andersen V, Bendixen G, Schiødt M, Oxholm P. A new model for classification of disease manifestations in primary Sjögren's syndrome: evaluation in a retrospective long-term study. Journal of internal medicine. 1996 Jun:239(6):475-82 [PubMed PMID: 8656140]
Level 2 (mid-level) evidenceSoto-Rojas AE, Villa AR, Sifuentes-Osornio J, Alarcón-Segovia D, Kraus A. Oral candidiasis and Sjögren's syndrome. The Journal of rheumatology. 1998 May:25(5):911-5 [PubMed PMID: 9598890]
Level 2 (mid-level) evidenceBronstein MN,Sokol RJ,Abman SH,Chatfield BA,Hammond KB,Hambidge KM,Stall CD,Accurso FJ, Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosis. The Journal of pediatrics. 1992 Apr; [PubMed PMID: 1552390]
Stathakis V, Kilkenny M, Marks R. Descriptive epidemiology of acne vulgaris in the community. The Australasian journal of dermatology. 1997 Aug:38(3):115-23 [PubMed PMID: 9293656]
Level 3 (low-level) evidenceZaenglein AL,Pathy AL,Schlosser BJ,Alikhan A,Baldwin HE,Berson DS,Bowe WP,Graber EM,Harper JC,Kang S,Keri JE,Leyden JJ,Reynolds RV,Silverberg NB,Stein Gold LF,Tollefson MM,Weiss JS,Dolan NC,Sagan AA,Stern M,Boyer KM,Bhushan R, Guidelines of care for the management of acne vulgaris. Journal of the American Academy of Dermatology. 2016 May; [PubMed PMID: 26897386]
Liu A, Yang DJ, Gerhardstein PC, Hsu S. Relapse of acne following isotretinoin treatment: a retrospective study of 405 patients. Journal of drugs in dermatology : JDD. 2008 Oct:7(10):963-6 [PubMed PMID: 19112761]
Level 2 (mid-level) evidence