Paper - Time and rate of loss of nuclei by the red blood cells of human embryos

From Embryology
Embryology - 25 May 2024    Facebook link Pinterest link Twitter link  Expand to Translate  
Google Translate - select your language from the list shown below (this will open a new external page)

العربية | català | 中文 | 中國傳統的 | français | Deutsche | עִברִית | हिंदी | bahasa Indonesia | italiano | 日本語 | 한국어 | မြန်မာ | Pilipino | Polskie | português | ਪੰਜਾਬੀ ਦੇ | Română | русский | Español | Swahili | Svensk | ไทย | Türkçe | اردو | ייִדיש | Tiếng Việt    These external translations are automated and may not be accurate. (More? About Translations)

Thompson E. Time and rate of loss of nuclei by the red blood cells of human embryos. (1951) Anat. Rec., 111: 317-325.

Online Editor  
Mark Hill.jpg
This historic 1951 paper by Thompson looks at the timeline of human development red blood cell development.

OTIS EM & BRENT R. (1954). Equivalent ages in mouse and human embryos. Anat. Rec. , 120, 33-63. PMID: 13207763
Modern Notes: blood

Cardiovascular Links: cardiovascular | Heart Tutorial | Lecture - Early Vascular | Lecture - Heart | Movies | 2016 Cardiac Review | heart | coronary circulation | heart valve | heart rate | Circulation | blood | blood vessel | blood vessel histology | heart histology | Lymphatic | ductus venosus | spleen | Stage 22 | cardiovascular abnormalities | OMIM | 2012 ECHO Meeting | Category:Cardiovascular
Historic Embryology - Cardiovascular 
1902 Vena cava inferior | 1905 Brain Blood Vessels | 1909 Cervical Veins | 1909 Dorsal aorta and umbilical veins | 1912 Heart | 1912 Human Heart | 1914 Earliest Blood-Vessels | 1915 Congenital Cardiac Disease | 1915 Dura Venous Sinuses | 1916 Blood cell origin | 1916 Pars Membranacea Septi | 1919 Lower Limb Arteries | 1921 Human Brain Vascular | 1921 Spleen | 1922 Aortic-Arch System | 1922 Pig Forelimb Arteries | 1922 Chicken Pulmonary | 1923 Head Subcutaneous Plexus | 1923 Ductus Venosus | 1925 Venous Development | 1927 Stage 11 Heart | 1928 Heart Blood Flow | 1935 Aorta | 1935 Venous valves | 1938 Pars Membranacea Septi | 1938 Foramen Ovale | 1939 Atrio-Ventricular Valves | 1940 Vena cava inferior | 1940 Early Hematopoiesis | 1941 Blood Formation | 1942 Truncus and Conus Partitioning | Ziegler Heart Models | 1951 Heart Movie | 1954 Week 9 Heart | 1957 Cranial venous system | 1959 Brain Arterial Anastomoses | Historic Embryology Papers | 2012 ECHO Meeting | 2016 Cardiac Review | Historic Disclaimer

Historic Disclaimer - information about historic embryology pages 
Mark Hill.jpg
Pages where the terms "Historic" (textbooks, papers, people, recommendations) appear on this site, and sections within pages where this disclaimer appears, indicate that the content and scientific understanding are specific to the time of publication. This means that while some scientific descriptions are still accurate, the terminology and interpretation of the developmental mechanisms reflect the understanding at the time of original publication and those of the preceding periods, these terms, interpretations and recommendations may not reflect our current scientific understanding.     (More? Embryology History | Historic Embryology Papers)

Time and Rate of Loss of Nuclei by the Red Blood Cells of Human Embryos

Elizabeth L. Thompson

Department of Anatomy, University of Michigan, Ann Arbor

One Figure


It has long been known that the earliest red corpuscles appearing in the circulating blood of young human embryos contain a nucleus. It has, also, been recognized that in older embryos none-nucleated red blood cells begin to appear in the heart and peripheral vessels, a condition effected, as in the adult, by the loss of the nuclei from existing cells. Many embryologists have noted the gradual change from this full compliment of nucleated red blood corpuscles in the young embryo to the late fetal condition of total or practically total loss of nuclei from these cells. Minot (in Keibel and Mall, ’12) reports that a considerable number of non—nucleated red blood cells were found in an embryo of two months, that this number increased consistently through tl1e third ‘month, and that at 8 months the majority of the corpusclcs were non—nucleated. Maximow (’27), Knoll (’29), Weintrobe and Schumaker (’36), Bloom (’38) and Bloom and Bartelmez (’40) and others discuss the histology of the hematopoietic centers and the various phases of blood development, including the fact that the red corpuscles in the early embryo are nucleated and that the later cells lack a nucleus. Specific information relative to the time and rate of the loss of nuclei from these cells is not given.

Most of the authors of recent textbooks of embryology give little-‘information as to the time when the loss of nuclei begins. Some fail even to mention it. Hamilton, Boyd and Mossman (’45) state only that the nuclei are extruded; Arey (’46) states that the non-nucleated red cells are first formed during the second month and that during the third month non-nucleated corpuscles first predominate. Jordan and Kindred (’48) state merely that in the human embryo nonnucleated erythrocytes are present late in the second month. Patten (’46) is somewhat more explicit as to the time of nuclear loss, having requested for citation some of the preliminary data on which this work is based. Two fairly definite time elements thus appear to have been established by previous workers, (1) that the loss of nuclei by the red blood cells begins to be evident during the second month in the human embryo and (2) that few nucleated red cells are found by the middle of the third month of intra-uterine life. The rate of loss of nuclei appears to be undetermined.

It became a matter of interest, therefore, to attempt to determine more precisely the age at which non-nucleated red cells first appear, the rate of increase of these cells, and the time at which the nucleated red cells disappear from the fetal circulation. To accomplish this end, red blood cell counts were made in 71 specimens from the Human Embryo Collection of the Anatomy Department of the University of Michigan Medical School. The embryos and fetuses used range in estimated age, from the beginning of the 5th Week (5 mm) to the 24th week (220 mm) (tables 1 and 2) and included all of the material in the collection which was sufficiently well preserved to make cell counts possible. Where conditions permitted a reasonable degree of accuracy, counts were made in the right atrium, in the aorta, and in a large vein, usually one of the cardinals. Ten counts of 100 cells each Were made from each of these regions. As a check on such routine counts, a sufficient number of samplings were made from smaller peripheral vessels to make certain there was no significant difference in the proportion of nucleated cells from internal as compared with more peripheral regions. This check was considered important because in some of the older fetuses, sectioned for regional study, only peripheral vessels were available. Vtlherever possible both arterial and venous vessels were used although the records show no appreciable difference in the cells from the two regions. Because of the known hematopoietic activity within the embryonic liver, no red cell counts were made from that area. Since the work here reported was concerned only with the time and rate of nuclear loss from the red blood cells, all cells encountered in the line of count, believed to be leucocytes Were excluded from the results. After making a number of counts, involving around 300 cells for each embryo, the results appeared significant enough to suggest the desirability of assembling them in the form of a graph. Such a graph based on the averages resulting from counting large numbers of cells in as many embryos of different ages as were available, should not only show the rate of nuclear loss but, during the period of active loss, it might also prove of value in estimating the approximate age of embryo fragments for which the usual methods were not feasible.

Table 1

Table 1 - Tabulated data relative to the loss of nuclei by red blood corpuscles in human embryos during the period of most rapid change
Embryo No. EH Size (mm CR) No. of Cells Counted Av. Non-Nuc. Cells per 100 Counted
Sixth Week
413 9.3 3,000 .00
382 9.5 3,000 .43
379 9.5 3,000 .13
336 10.3 3,000 .10
200 11 2,000 .10
88 11 3,000 .13
266 11 3,000 .16
253 11.2 3,000 .10
271 11.4 3,000 .13
267 12 3,000 .10
262 12.5 3,000 .23
Seventh week
342 13 3,000 .20
252 13.7 3,000 .33
407 14.5 3,000 .10
314 14.8 3,000 .06
194 15 3,000 .13
227 15 3,000 .30
303 15.1 3,000 .16
442 17 3,000 .93
249 15.7 3,000 .36
138 18 3,000 .13
Eighth week
4 (Adjusted age) 18-19 3,000 1.80
353 19 3,000 3.60
253 20 3,000 4.23
420 20.5 3,000 3.76
231 21 3,000 5.13
33 23 3,000 5.26
237 20 3,000 12.03
240 28 3,000 30.90
Ninth week
15 30 3,000 63.40
47 32 3,000 65.53
217 33 3,000 67.30
22 33 3,000 70.00
17 39 3,000 74.13
Tenth week
49 47 3,000 94.50
Eleventh week
370(5) 54 1,000 99.80
312(1)) 54 3,000 99.50
331(0) 55 3,000 97.80
23 60 3,000 96.90
74 60 1,000 97.3
173(k) 65 2,000 98.55

The counts used in constructing the tables and the graph ranged from 1,000 to 3,000 blood cells for each embryo having blood well enough preserved to permit counting. The larger number (3,000) was obtained Wherever possible. The total number of cells counted in the 71 embryos used was 183,000 (table 2). Certain precautions Were taken in order to insure greater accuracy in the results: (1) Where possible 1,000 cells were counted from each of three different areas in the embryo: (2) cells were counted from alternate sections in each series, in order to avoid the chance of counting some of the same cells twice a.s might occur in counting cells cut in sectioning and thus appearing in consecutive sections; (3) relatively large numbers of cells (1,000 to 3,000) were counted from different areas in each embryo or fetus in order to reduce the errors involved in the non-uniform distribution of nucleated and non-nucleated cells or plastids; (4) the averages used (table 1) in plotting the curve, were based on the total number of cells counted (1,000 to 3,000) in each embryo; (5) as a further attempt to reduce errors, an occasional embryo was recounted after having been put aside for a time, these recounts were close enough to the originals to indicate that there had been no significant errors in the counts as a whole; (6) the embryos used for counting were not arranged in chronological sequence but were selected at random and the age range relations of the results obtained were not correlated until a later date.

Table 2

Table 2 - Condensed data relative to the loss of nuclei by red blood corpuscles in all embryos used in this study
Developmental Age Number of Embryos Used Total No. of
Cells Counted
Av. Non-Nuc. Cells
per 100 Counted
5th week 6 12,000 .00
6th week 16 46,000 .09
7th week 10 30,000 .42
8th Week 8 24,000 9.09
9th week 5 15,000 69.23
10th week 1 3,000 94.50
11th week 0 13,000 97.81
12th week 1 2,000 97.7
13th week 2 5,000 99.25
14th week 6 13,000 99.27
15th week 2 4,000 99.9?
16th week 1 1,000 98.40
17th week 2 4,000 99.70
18th Week 1 2,000 99.95
19th Week 2 4,000 99.82
22nd Week 1 3,000 99.90
24th week 1 2,000 99.80
Totals 71 183,000

The embryos used were catalogued according to 0.1%. meas-. urcments taken at the time of receipt (usually shortly after fixation). For the purposes of this Work, these measurements have been interpreted in terms of Weeks (fertilization age) with the aid of the table and curves in Patten’s Human Embryology (’46) pp. 184-185. All such measurements are, of course, subject to minor errors and these may well account ‘for some of the Variations in the cell counts. One such discrepancy was so marked (EH 4, 15 mm) that the sections were checked for age with data recorded by Streeter (’48). Using his criteria, this embryo was judged to be older than the catalogued measurement indicated. As a further check, measurements of the sectioned embryo were made as suggested by Patten and Philpott (’21). Allowing for shrinkage due to fixation, these measurements suggested an older embryo. The results of these two checks together with the condition of nucleation of the red blood corpuscles indicated a measurement of 18-19 mm and this adjusted age (from the 7th week to early in the 8th week) has been used in the records given here (tables 1 and 2). It is interesting to note that the cheek methods used were in reasonable agreement suggesting that the condition of nucleation of the red blood cells may be used to approximate the age of embryos during the period when nuclear loss is progressing rapidly (7th through 10th week) (fig. 1).

In the entire course of the work no non-nucleated cells were observed in embryos of less than 9 mm C—R. A very few, that is an average of about 0.1%, appeared in the 6th week. Em» bryos in the 7th week of development showed a slight rise in the number of non~nucleated red blood cells, the average being about 0.5%. This number began to increase rapidly during the 8th week, by the end of which the non—nucleated red cells had risen to 9%. The most rapid change occurred in embryos during the 9th week of development. At the end of this week the non-nucleated cells have reached an average of 69%, an increase of 60% over embryos at the end of the 8th week. Embryos in the 10th week of development showed a further average. increase of 25% in non—nucleated red blood cells, so that by the end of that week the average count was about 94% of non—nucleated cells. By the 11th week when the average number of non—nucleated corpuscles was 97.8%, the changesin the average number of anucleate red blood cells became negligible, reaching a final 99.8% non—nucleated red cells in the 24th week (table 2).

The graph plotted from the data in table 1 and based directly on the average increase in nuclear loss per week, shows vividly the relatively slow loss of nuclei from the red blood cells between the 6th week and late in the 7th week, which is followed by a more marked change in the nuclear condition between the latter part of the 7th and the 8th weeks. The period of pronounced loss extends into the 10th Week. In the next two weeks the rate of loss slows abruptly. Beyond this period the averages were not plotted. As was shown in table 2 there was little variation from then until the 24th week. Although the ages of the embryos used are not as uniformly distributed in the entire group as one might wish, it is believed that the total number (71) of embryos used (table 2) is sufficiently large to give the recorded data (table 1) some significance. The relatively large number of cells (1,0003,000) counted for each embryo aids in reducing errors in the counts averaged and used in plotting the curve.

Thompson1951 fig01.jpg

Fig. 1 Graph showing the rate of loss of nuclei by red blood corpuscles in human embryo during the period of most rapid change. The vertical axis shows the average number of non-nucleated red blood corpuscles per 100 for embryos in the age groups indicated on the horizontal axis. It is based on data recorded in table 1.

It is believed that this curve, which indicates the weekly rate of nuclear loss by the red blood corpuscles in human embryos, will prove to be of value in determining the age of certain embryos which have been inadequately or inaccurately measured. It will also add another factor useful in determining the developmental stages of human embryos as described by Streeter (’45, ’48). It is quite possible that the data and graph might prove of value in estimating the age of embryos too fragmented, or otherwise multilated, to permit the making of accurate measurements or the study of the developmental characteristics used by Streeter. Enough blood in an embryonic fragment, sufficiently well preserved so that nucleated and non-nucleated cells could be distinguished, would be all that was required to fix age fairly accurately in the case of embryos in the periods of rapid nuclear loss.

Literature Cited

Arey, LESLIE B. 1946 Developmental anatomy. ix + 616 pp. W. B. Saunders 00., Philadelphia.

BLOOM, Vi»7ILLI£LM 1938 Erythrogenesis of mammalian blood. In Handbook of hematology, Hal Downey, editor. W. B. Saunders 00., Philadelphia, 2: 865-922.

Bloom W. and Bartelmez GW. Hematopoiesis in young human embryos. (1940) Amer. J Anat., 67, 21-53.

HAMILTON, W. J., F. D. Born AND H. W. MOSSMAN 1945 Human embryology. viii + 366 pp. The Williams and Wilkins 00., Baltimore.

JORDAN, HARVEY E., AND JAMES E. KINDRED 1948 Textbook of embryology. xiv + 613 pp. D. Appleton~0entury 00., New York.

KNOLL, W. 1929 Untersuehungen fiber embryonali Blutbildung beim Menchen. Jahr 6. Morph. 11. mikrosk. Anat., Abt. 2. Zeitschr. Mikrosk. Aunt. 13 (13): 199-232.

MAXIMOW, A. 1927 Bindegewebe und blutbildende Gewebe. Handbueh. d. mikr. Anat. d. Mensehen. (V. Mfillendofi), Berlin, 2: 232.

Minot CS. The origin of the angioblast and the development of the blood. (1912)Sect. I, chapt. 18, vol. 2, in Keibel F. and Mall FP. Manual of Human Embryology II. (1912) J. B. Lippincott Company, Philadelphia..

PATTEN, BRADLEY, M. 1946 Human embryology. XV + 776 pp. Blakiston Co., Philadelphia.

PATTEN, BRADLEY 14., sub REES PHILPOTT 1921 The shrinkage of embryos in the processes preparatory to sectioning. Anat. Rec., 20: 4, 393-413.

STREETER, G. L. 1945 Developmental horizons in human embryos. Age groups XIII and XIV. Carnegie Gontrib. to E1nbryo1., 31: 29-63.

  • 1948 Developmental horizons in human embryos. Age groups XV—— XVIII. Carnegie Contrib. to Embry01., 32: 133-203.

WINTROBE, M. M. 1936 Erythrocyte studies in the mammalian fetus and newborn. Am. J. Anat., 58: 313——328.

Cite this page: Hill, M.A. (2024, May 25) Embryology Paper - Time and rate of loss of nuclei by the red blood cells of human embryos. Retrieved from

What Links Here?
© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G